Linked Data
ClinVar Variation Id:
2087397
ClinVar RCV Id:
RCV003009539
dbSNP Id:
rs1586069412
MyVariant Identifiers:
chr8:g.77895776G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.76983540G>A , CM000670.2:g.76983540G>A | GRCh38 |
| NC_000008.10:g.77895776G>A , CM000670.1:g.77895776G>A | GRCh37 |
| NC_000008.9:g.78058331G>A | NCBI36 |
| NG_008371.1:g.21749C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000357039.9:c.639C>T MANE Select | ENSP00000349543.4:p.Val213= | |
| ENST00000357039.8:c.639C>T | ENSP00000349543.4:p.Val213= | |
| ENST00000520103.5:c.639C>T | ENSP00000428590.1:p.Val213= | |
| ENST00000522527.5:c.639C>T | ENSP00000428638.1:p.Val213= | |
| NM_000318.2:c.639C>T | NP_000309.1:p.Val213= | |
| NM_001079867.1:c.639C>T | NP_001073336.1:p.Val213= | |
| NM_001172086.1:c.639C>T | NP_001165557.1:p.Val213= | |
| NM_001172087.1:c.639C>T | NP_001165558.1:p.Val213= | |
| NM_000318.3:c.639C>T MANE Select | NP_000309.2:p.Val213= | |
| NM_001079867.2:c.639C>T | NP_001073336.2:p.Val213= | |
| NM_001172086.2:c.639C>T | NP_001165557.2:p.Val213= | |
| NM_001172087.2:c.639C>T | NP_001165558.2:p.Val213= |