Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43048426A>T , CM000677.2:g.43048426A>T | GRCh38 |
| NC_000015.9:g.43340624A>T , CM000677.1:g.43340624A>T | GRCh37 |
| NC_000015.8:g.41127916A>T | NCBI36 |
| NG_012182.1:g.62663T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290650.9:c.1505T>A MANE Select | ENSP00000290650.4:p.Phe502Tyr | |
| ENST00000290650.8:c.1505T>A | ENSP00000290650.4:p.Phe502Tyr | |
| ENST00000546274.6:c.1505T>A | ENSP00000477932.1:p.Phe502Tyr | |
| ENST00000563239.1:c.*203-1137T>A | ENSP00000456502.1:n.*203-1137T>A | |
| ENST00000569971.5:c.376T>A | ENSP00000455759.1:n.376T>A | |
| NM_174916.2:c.1505T>A | NP_777576.1:p.Phe502Tyr | |
| NM_174916.3:c.1505T>A MANE Select | NP_777576.1:p.Phe502Tyr |