LINC00612 long intergenic non-protein coding RNA 612
Information
- Symbol
- LINC00612
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 612
- Entrez Gene ID
- 253128
- Genome
- hg19
- Position
- chr12:9,208,199-9,217,648
- Genome
- hg38
- Position
- chr12:9,055,603-9,065,052
- HGNC
- HGNC:28621 HGNC
- Ensembl
- ENSG00000214851 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[No Data.]
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 |
Type | ID |
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SYNONYM | C12orf33 |
HGNC | HGNC:28621 HGNC |
Ensembl | ENSG00000214851 Ensembl |
AllianceGenome | HGNC:28621 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000538094.2 | hg38 | chr12 | 9,055,589 | 9,065,070 | 9,482 |
ENST00000675544.1 | hg38 | chr12 | 9,055,603 | 9,065,052 | 9,450 |
ENST00000538094.2 | hg19 | chr12 | 9,208,185 | 9,217,666 | 9,482 |
ENST00000675544.1 | hg19 | chr12 | 9,208,199 | 9,217,648 | 9,450 |
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