Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232541493T>A , CM000664.2:g.232541493T>A | GRCh38 |
| NC_000002.11:g.233406203T>A , CM000664.1:g.233406203T>A | GRCh37 |
| NC_000002.10:g.233114447T>A | NCBI36 |
| NG_012954.1:g.6767T>A | |
| NG_012954.2:g.6802T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651502.1:c.470T>A MANE Select | ENSP00000498757.1:p.Phe157Tyr | |
| ENST00000389492.3:c.350+782T>A | ENSP00000374143.3:n.350+782T>A | |
| ENST00000389494.7:c.470T>A | ENSP00000374145.3:p.Phe157Tyr | |
| ENST00000485094.1:n.491T>A | ||
| NM_005199.4:c.470T>A | NP_005190.4:p.Phe157Tyr | |
| NM_005199.5:c.470T>A MANE Select | NP_005190.4:p.Phe157Tyr |