Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44118516A>T , CM000682.2:g.44118516A>T | GRCh38 |
| NC_000020.10:g.42747156A>T , CM000682.1:g.42747156A>T | GRCh37 |
| NC_000020.9:g.42180570A>T | NCBI36 |
| NG_031867.1:g.74063T>A , LRG_394:g.74063T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020433.5:c.1277T>A MANE Select | NP_065166.2:p.Phe426Tyr |
| ENST00000372980.4:c.1277T>A MANE Select | ENSP00000362071.3:p.Phe426Tyr |
| NM_020433.4:c.1277T>A , LRG_394t1:c.1277T>A | NP_065166.2:p.Phe426Tyr |
| ENST00000372980.3:c.1277T>A | ENSP00000362071.3:p.Phe426Tyr |
| XM_006723832.2:c.1277T>A | XP_006723895.1:p.Phe426Tyr |