Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174724799T>A , CM000667.2:g.174724799T>A | GRCh38 |
| NC_000005.9:g.174151802T>A , CM000667.1:g.174151802T>A | GRCh37 |
| NC_000005.8:g.174084408T>A | NCBI36 |
| NG_008124.1:g.5228T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.140T>A MANE Select | ENSP00000239243.5:p.Phe47Tyr | |
| ENST00000239243.6:c.140T>A | ENSP00000239243.5:p.Phe47Tyr | |
| ENST00000507785.2:c.140T>A | ENSP00000427425.1:p.Phe47Tyr | |
| NM_002449.4:c.140T>A | NP_002440.2:p.Phe47Tyr | |
| NM_001363626.1:c.140T>A | NP_001350555.1:p.Phe47Tyr | |
| NM_002449.5:c.140T>A MANE Select | NP_002440.2:p.Phe47Tyr | |
| NM_001363626.2:c.140T>A | NP_001350555.1:p.Phe47Tyr |