Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21011799A>T , CM000664.2:g.21011799A>T | GRCh38 |
| NC_000002.11:g.21234671A>T , CM000664.1:g.21234671A>T | GRCh37 |
| NC_000002.10:g.21088176A>T | NCBI36 |
| NG_011793.1:g.37275T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673739.2:c.*4375T>A | ENSP00000501110.2:n.*4375T>A | |
| ENST00000673739.1:c.4783T>A | ENSP00000501110.1:n.4783T>A | |
| ENST00000233242.5:c.5069T>A MANE Select | ENSP00000233242.1:p.Phe1690Tyr | |
| ENST00000616098.4:c.5069T>A | ENSP00000477990.1:p.Phe1690Tyr | |
| NM_000384.2:c.5069T>A | NP_000375.2:p.Phe1690Tyr | |
| XM_011532809.1:c.5069T>A | XP_011531111.1:p.Phe1690Tyr | |
| NM_000384.3:c.5069T>A MANE Select | NP_000375.3:p.Phe1690Tyr |