Linked Data
ClinVar Variation Id:
1423839
ClinVar RCV Id:
RCV001929131
dbSNP Id:
rs779699586
gnomAD v2:
12-5155075-G-A
gnomAD v4:
12-5045909-G-A
COSMIC:
COSM1470582
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5045909G>A , CM000674.2:g.5045909G>A | GRCh38 |
| NC_000012.11:g.5155075G>A , CM000674.1:g.5155075G>A | GRCh37 |
| NC_000012.10:g.5025336G>A | NCBI36 |
| NG_012198.1:g.6991G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.1762G>A MANE Select | ENSP00000252321.3:p.Val588Ile | |
| ENST00000252321.4:c.1762G>A | ENSP00000252321.3:p.Val588Ile | |
| NM_002234.3:c.1762G>A | NP_002225.2:p.Val588Ile | |
| NM_002234.4:c.1762G>A MANE Select | NP_002225.2:p.Val588Ile |