Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52514985A>T , CM000674.2:g.52514985A>T | GRCh38 |
| NC_000012.11:g.52908769A>T , CM000674.1:g.52908769A>T | GRCh37 |
| NC_000012.10:g.51195036A>T | NCBI36 |
| NG_008297.1:g.10475T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.1730T>A MANE Select | ENSP00000252242.4:p.Phe577Tyr | |
| ENST00000252242.8:c.1730T>A | ENSP00000252242.4:p.Phe577Tyr | |
| NM_000424.3:c.1730T>A | NP_000415.2:p.Phe577Tyr | |
| NM_000424.4:c.1730T>A MANE Select | NP_000415.2:p.Phe577Tyr |