Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.43030461T>A , CM000666.2:g.43030461T>A | GRCh38 |
| NC_000004.11:g.43032478T>A , CM000666.1:g.43032478T>A | GRCh37 |
| NC_000004.10:g.42727235T>A | NCBI36 |
| NG_027718.1:g.142196T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080476.3:c.794T>A MANE Select | NP_001073945.1:p.Phe265Tyr |
| ENST00000399770.3:c.794T>A MANE Select | ENSP00000382670.2:p.Phe265Tyr |
| NM_001080476.2:c.794T>A | NP_001073945.1:p.Phe265Tyr |
| ENST00000399770.2:c.794T>A | ENSP00000382670.2:p.Phe265Tyr |
| XM_011513691.1:c.431T>A | XP_011511993.1:p.Phe144Tyr |