LINC02028 long intergenic non-protein coding RNA 2028
Information
- Symbol
- LINC02028
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2028
- Entrez Gene ID
- 285389
- Genome
- hg19
- Position
- chr3:193,766,709-193,787,318
- Genome
- hg38
- Position
- chr3:194,048,920-194,069,529
- HGNC
- HGNC:27718 HGNC
- Ensembl
- ENSG00000230102 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000593326.6 | hg38 | chr3 | 194,042,910 | 194,069,553 | 26,644 |
ENST00000432154.5 | hg38 | chr3 | 194,048,920 | 194,069,529 | 20,610 |
ENST00000420947.3 | hg38 | chr3 | 194,015,443 | 194,057,679 | 42,237 |
ENST00000622169.5 | hg38 | chr3 | 194,005,259 | 194,058,461 | 53,203 |
ENST00000656867.1 | hg38 | chr3 | 194,009,954 | 194,058,467 | 48,514 |
ENST00000670206.1 | hg38 | chr3 | 194,042,909 | 194,069,577 | 26,669 |
ENST00000665835.1 | hg38 | chr3 | 194,036,331 | 194,058,429 | 22,099 |
ENST00000656099.1 | hg38 | chr3 | 194,009,449 | 194,047,197 | 37,749 |
ENST00000622169.5 | hg19 | chr3 | 193,723,048 | 193,776,250 | 53,203 |
ENST00000420947.3 | hg19 | chr3 | 193,733,232 | 193,775,468 | 42,237 |
ENST00000593326.6 | hg19 | chr3 | 193,760,699 | 193,787,342 | 26,644 |
ENST00000432154.5 | hg19 | chr3 | 193,766,709 | 193,787,318 | 20,610 |
ENST00000665835.1 | hg19 | chr3 | 193,754,120 | 193,776,218 | 22,099 |
ENST00000670206.1 | hg19 | chr3 | 193,760,698 | 193,787,366 | 26,669 |
ENST00000656099.1 | hg19 | chr3 | 193,727,238 | 193,764,986 | 37,749 |
ENST00000656867.1 | hg19 | chr3 | 193,727,743 | 193,776,256 | 48,514 |
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