HRG-AS1 HRG and FETUB antisense RNA 1
Information
- Symbol
- HRG-AS1
- Type
- ncRNA
- Description
- HRG and FETUB antisense RNA 1
- Entrez Gene ID
- 105374258
- Genome
- hg19
- Position
- chr3:186,359,324-186,413,771
- Genome
- hg38
- Position
- chr3:186,641,535-186,695,982
- HGNC
- HGNC:55915 HGNC
- Ensembl
- ENSG00000197099 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Ranking
ClinVar | |
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0 |
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Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000630315.2 | hg38 | chr3 | 186,641,535 | 186,695,982 | 54,448 |
ENST00000626006.2 | hg38 | chr3 | 186,666,931 | 186,674,518 | 7,588 |
ENST00000599314.5 | hg38 | chr3 | 186,717,249 | 186,757,668 | 40,420 |
ENST00000455926.3 | hg38 | chr3 | 186,641,515 | 186,665,703 | 24,189 |
ENST00000354642.4 | hg38 | chr3 | 186,714,448 | 186,746,130 | 31,683 |
ENST00000625877.1 | hg38 | chr3 | 186,668,641 | 186,703,106 | 34,466 |
ENST00000625826.1 | hg38 | chr3 | 186,651,311 | 186,668,912 | 17,602 |
ENST00000630726.2 | hg38 | chr3 | 186,651,812 | 186,718,504 | 66,693 |
ENST00000630331.2 | hg38 | chr3 | 186,647,113 | 186,743,756 | 96,644 |
ENST00000428501.5 | hg38 | chr3 | 186,641,510 | 186,665,707 | 24,198 |
ENST00000608173.2 | hg38 | chr3 | 186,757,025 | 186,760,541 | 3,517 |
ENST00000626649.2 | hg38 | chr3 | 186,641,539 | 186,710,567 | 69,029 |
ENST00000428501.5 | hg19 | chr3 | 186,359,299 | 186,383,496 | 24,198 |
ENST00000455926.3 | hg19 | chr3 | 186,359,304 | 186,383,492 | 24,189 |
ENST00000354642.4 | hg19 | chr3 | 186,432,237 | 186,463,919 | 31,683 |
ENST00000599314.5 | hg19 | chr3 | 186,435,038 | 186,475,457 | 40,420 |
ENST00000608173.2 | hg19 | chr3 | 186,474,814 | 186,478,330 | 3,517 |
ENST00000630315.2 | hg19 | chr3 | 186,359,324 | 186,413,771 | 54,448 |
ENST00000626649.2 | hg19 | chr3 | 186,359,328 | 186,428,356 | 69,029 |
ENST00000630331.2 | hg19 | chr3 | 186,364,902 | 186,461,545 | 96,644 |
ENST00000625826.1 | hg19 | chr3 | 186,369,100 | 186,386,701 | 17,602 |
ENST00000630726.2 | hg19 | chr3 | 186,369,601 | 186,436,293 | 66,693 |
ENST00000626006.2 | hg19 | chr3 | 186,384,720 | 186,392,307 | 7,588 |
ENST00000625877.1 | hg19 | chr3 | 186,386,430 | 186,420,895 | 34,466 |
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