Linked Data
ClinVar Variation Id:
2736231
ClinVar RCV Id:
RCV003559866
dbSNP Id:
rs890956501
gnomAD v2:
15-72103849-G-A
gnomAD v4:
15-71811509-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.71811509G>A , CM000677.2:g.71811509G>A | GRCh38 |
| NC_000015.9:g.72103849G>A , CM000677.1:g.72103849G>A | GRCh37 |
| NC_000015.8:g.69890903G>A | NCBI36 |
| NG_009113.2:g.5955G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617575.5:c.145G>A MANE Select | ENSP00000482504.1:p.Val49Met | |
| ENST00000617575.4:c.145G>A | ENSP00000482504.1:p.Val49Met | |
| ENST00000621098.1:c.145G>A | ENSP00000479962.1:p.Val49Met | |
| ENST00000621736.4:c.-120G>A | ENSP00000479254.1:n.-120G>A | |
| NM_014249.3:c.145G>A | NP_055064.1:p.Val49Met | |
| NM_016346.3:c.145G>A | NP_057430.1:p.Val49Met | |
| XM_011521146.1:c.-120G>A | XP_011519448.1:n.-120G>A | |
| NM_014249.4:c.145G>A MANE Select | NP_055064.1:p.Val49Met | |
| NM_016346.4:c.145G>A | NP_057430.1:p.Val49Met |