Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240872982C>A , CM000664.2:g.240872982C>A | GRCh38 |
| NC_000002.11:g.241812399C>A , CM000664.1:g.241812399C>A | GRCh37 |
| NC_000002.10:g.241461072C>A | NCBI36 |
| NG_008005.1:g.9238C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000030.3:c.528C>A MANE Select | NP_000021.1:p.Tyr176Ter |
| ENST00000307503.4:c.528C>A MANE Select | ENSP00000302620.3:p.Tyr176Ter |
| NM_000030.2:c.528C>A | NP_000021.1:p.Tyr176Ter |
| ENST00000307503.3:c.528C>A | ENSP00000302620.3:p.Tyr176Ter |
| ENST00000472436.1:n.548C>A | |
| ENST00000476698.1:n.265C>A |