Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47839841T>A , CM000681.2:g.47839841T>A | GRCh38 |
| NC_000019.9:g.48343098T>A , CM000681.1:g.48343098T>A | GRCh37 |
| NC_000019.8:g.53034910T>A | NCBI36 |
| NG_008605.1:g.23000T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000554.6:c.774T>A MANE Select | NP_000545.1:p.Tyr258Ter |
| ENST00000221996.12:c.774T>A MANE Select | ENSP00000221996.5:p.Tyr258Ter |
| NM_000554.4:c.774T>A | NP_000545.1:p.Tyr258Ter |
| NM_000554.5:c.774T>A | NP_000545.1:p.Tyr258Ter |
| ENST00000221996.11:c.774T>A | ENSP00000221996.5:p.Tyr258Ter |
| ENST00000539067.5:c.774T>A | ENSP00000445565.1:p.Tyr258Ter |
| ENST00000613299.1:c.*496T>A | ENSP00000478106.1:n.*496T>A |