Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221716A>T , CM000671.2:g.99221716A>T | GRCh38 |
| NC_000009.11:g.101983998A>T , CM000671.1:g.101983998A>T | GRCh37 |
| NC_000009.10:g.101023819A>T | NCBI36 |
| NG_008928.1:g.5249T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_033087.4:c.179T>A MANE Select | NP_149078.1:p.Phe60Tyr |
| ENST00000476832.2:c.179T>A MANE Select | ENSP00000417764.1:p.Phe60Tyr |
| NM_033087.3:c.179T>A | NP_149078.1:p.Phe60Tyr |
| NR_024532.1:n.249T>A | |
| NR_024532.2:n.227T>A | |
| ENST00000238477.5:c.179T>A | ENSP00000432675.2:p.Phe60Tyr |
| ENST00000476832.1:c.179T>A | ENSP00000417764.1:p.Phe60Tyr |