Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47839730C>A , CM000681.2:g.47839730C>A | GRCh38 |
| NC_000019.9:g.48342987C>A , CM000681.1:g.48342987C>A | GRCh37 |
| NC_000019.8:g.53034799C>A | NCBI36 |
| NG_008605.1:g.22889C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221996.12:c.663C>A MANE Select | ENSP00000221996.5:p.Tyr221Ter | |
| ENST00000221996.11:c.663C>A | ENSP00000221996.5:p.Tyr221Ter | |
| ENST00000539067.5:c.663C>A | ENSP00000445565.1:p.Tyr221Ter | |
| ENST00000613299.1:c.*385C>A | ENSP00000478106.1:n.*385C>A | |
| NM_000554.4:c.663C>A | NP_000545.1:p.Tyr221Ter | |
| NM_000554.5:c.663C>A | NP_000545.1:p.Tyr221Ter | |
| NM_000554.6:c.663C>A MANE Select | NP_000545.1:p.Tyr221Ter |