Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178014450A>T , CM000664.2:g.178014450A>T | GRCh38 |
| NC_000002.11:g.178879177A>T , CM000664.1:g.178879177A>T | GRCh37 |
| NC_000002.10:g.178587423A>T | NCBI36 |
| NG_012168.1:g.98890T>A | |
| NG_012168.2:g.98890T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286063.11:c.923T>A MANE Select | ENSP00000286063.5:p.Phe308Tyr | |
| ENST00000286063.10:c.923T>A | ENSP00000286063.5:p.Phe308Tyr | |
| ENST00000358450.8:c.173T>A | ENSP00000351232.4:p.Phe58Tyr | |
| NM_001077197.1:c.173T>A | NP_001070665.1:p.Phe58Tyr | |
| NM_016953.3:c.923T>A | NP_058649.3:p.Phe308Tyr | |
| NM_016953.4:c.923T>A MANE Select | NP_058649.3:p.Phe308Tyr | |
| NM_001077197.2:c.173T>A | NP_001070665.1:p.Phe58Tyr |