Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.71811957G>A , CM000677.2:g.71811957G>A | GRCh38 |
| NC_000015.9:g.72104297G>A , CM000677.1:g.72104297G>A | GRCh37 |
| NC_000015.8:g.69891351G>A | NCBI36 |
| NG_009113.2:g.6403G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014249.4:c.352G>A MANE Select | NP_055064.1:p.Val118Met |
| ENST00000617575.5:c.352G>A MANE Select | ENSP00000482504.1:p.Val118Met |
| NM_014249.3:c.352G>A | NP_055064.1:p.Val118Met |
| NM_016346.3:c.352G>A | NP_057430.1:p.Val118Met |
| NM_016346.4:c.352G>A | NP_057430.1:p.Val118Met |
| ENST00000617575.4:c.352G>A | ENSP00000482504.1:p.Val118Met |
| ENST00000621098.1:c.352G>A | ENSP00000479962.1:p.Val118Met |
| ENST00000621736.4:c.88G>A | ENSP00000479254.1:p.Val30Met |
| XM_011521146.1:c.88G>A | XP_011519448.1:p.Val30Met |