Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38692306T>A , CM000675.2:g.38692306T>A | GRCh38 |
| NC_000013.10:g.39266443T>A , CM000675.1:g.39266443T>A | GRCh37 |
| NC_000013.9:g.38164443T>A | NCBI36 |
| NG_008125.2:g.10271T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.4962T>A MANE Select | NP_997244.4:p.Ser1654Arg |
| ENST00000280481.9:c.4962T>A MANE Select | ENSP00000280481.7:p.Ser1654Arg |
| NM_207361.5:c.4962T>A | NP_997244.4:p.Ser1654Arg |
| ENST00000280481.8:c.4962T>A | ENSP00000280481.7:p.Ser1654Arg |
| XM_011535057.1:c.4962T>A | XP_011533359.1:p.Ser1654Arg |
| XM_017020554.1:c.4962T>A | XP_016876043.1:p.Ser1654Arg |
| XR_941571.1:n.5270T>A | |
| XR_941571.2:n.5266T>A |