Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154901439C>T , CM000685.2:g.154901439C>T | GRCh38 |
| NC_000023.10:g.154129714C>T , CM000685.1:g.154129714C>T | GRCh37 |
| NC_000023.9:g.153782908C>T | NCBI36 |
| NG_011403.1:g.126285G>A | |
| NG_011403.2:g.126285G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.6119G>A MANE Select | NP_000123.1:p.Cys2040Tyr |
| ENST00000360256.9:c.6119G>A MANE Select | ENSP00000353393.4:p.Cys2040Tyr |
| NM_000132.3:c.6119G>A | NP_000123.1:p.Cys2040Tyr |
| ENST00000360256.8:c.6119G>A | ENSP00000353393.4:p.Cys2040Tyr |
| XM_011531126.1:c.6014G>A | XP_011529428.1:p.Cys2005Tyr |