Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586646G>A , CM000679.2:g.41586646G>A | GRCh38 |
| NC_000017.10:g.39742898G>A , CM000679.1:g.39742898G>A | GRCh37 |
| NC_000017.9:g.36996424G>A | NCBI36 |
| NG_008624.1:g.5250C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000526.5:c.189C>T MANE Select | NP_000517.3:p.Cys63= |
| ENST00000167586.7:c.189C>T MANE Select | ENSP00000167586.6:p.Cys63= |
| NM_000526.4:c.189C>T | NP_000517.2:p.Tyr63= |
| ENST00000167586.6:c.189C>T | ENSP00000167586.6:p.Cys63= |