Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.164996760A>T , CM000665.2:g.164996760A>T | GRCh38 |
| NC_000003.11:g.164714548A>T , CM000665.1:g.164714548A>T | GRCh37 |
| NC_000003.10:g.166197242A>T | NCBI36 |
| NG_017043.1:g.86736T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264382.8:c.4553T>A MANE Select | ENSP00000264382.3:p.Phe1518Tyr | |
| ENST00000264382.7:c.4553T>A | ENSP00000264382.3:p.Phe1518Tyr | |
| NM_001041.3:c.4553T>A | NP_001032.2:p.Phe1518Tyr | |
| XM_011513078.1:c.4454T>A | XP_011511380.1:p.Phe1485Tyr | |
| XM_011513078.2:c.4454T>A | XP_011511380.1:p.Phe1485Tyr | |
| NM_001041.4:c.4553T>A MANE Select | NP_001032.2:p.Phe1518Tyr |