Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112228629T>A , CM000673.2:g.112228629T>A | GRCh38 |
| NC_000011.9:g.112099352T>A , CM000673.1:g.112099352T>A | GRCh37 |
| NC_000011.8:g.111604562T>A | NCBI36 |
| NG_008743.1:g.7265T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000280362.8:c.119T>A MANE Select | ENSP00000280362.3:p.Phe40Tyr | |
| ENST00000280362.7:c.119T>A | ENSP00000280362.3:p.Phe40Tyr | |
| ENST00000524931.1:c.-86T>A | ENSP00000434688.1:n.-86T>A | |
| ENST00000525645.1:n.194T>A | ||
| ENST00000525803.1:c.119T>A | ENSP00000431750.1:p.Phe40Tyr | |
| ENST00000528679.5:c.119T>A | ENSP00000435895.1:p.Phe40Tyr | |
| ENST00000531673.5:c.119T>A | ENSP00000433469.1:p.Phe40Tyr | |
| NM_000317.2:c.119T>A | NP_000308.1:p.Phe40Tyr | |
| NM_000317.3:c.119T>A MANE Select | NP_000308.1:p.Phe40Tyr |