Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15442462C>A , CM000663.2:g.15442462C>A | GRCh38 |
| NC_000001.10:g.15768958C>A , CM000663.1:g.15768958C>A | GRCh37 |
| NC_000001.9:g.15641545C>A | NCBI36 |
| NG_009253.1:g.9021C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007272.3:c.246C>A MANE Select | NP_009203.2:p.Tyr82Ter |
| ENST00000375949.5:c.246C>A MANE Select | ENSP00000365116.4:p.Tyr82Ter |
| NM_007272.2:c.246C>A | NP_009203.2:p.Tyr82Ter |
| ENST00000375943.6:c.56C>A | ENSP00000365110.2:p.Thr19Asn |
| ENST00000375949.4:c.246C>A | ENSP00000365116.4:p.Tyr82Ter |
| ENST00000476813.5:n.68C>A | |
| ENST00000483406.1:n.156C>A | |
| XM_011540550.1:c.246C>A | XP_011538852.1:p.Tyr82Ter |