Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47733711T>A , CM000679.2:g.47733711T>A | GRCh38 |
| NC_000017.10:g.45811077T>A , CM000679.1:g.45811077T>A | GRCh37 |
| NC_000017.9:g.43166076T>A | NCBI36 |
| NG_012166.1:g.5468T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.257T>A MANE Select | ENSP00000177694.1:p.Phe86Tyr | |
| ENST00000177694.1:c.257T>A | ENSP00000177694.1:p.Phe86Tyr | |
| ENST00000581328.1:n.287T>A | ||
| NM_013351.1:c.257T>A | NP_037483.1:p.Phe86Tyr | |
| XM_011524698.1:c.257T>A | XP_011523000.1:p.Phe86Tyr | |
| NM_013351.2:c.257T>A MANE Select | NP_037483.1:p.Phe86Tyr |