Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541914A>T , CM000663.2:g.169541914A>T | GRCh38 |
| NC_000001.10:g.169511152A>T , CM000663.1:g.169511152A>T | GRCh37 |
| NC_000001.9:g.167777776A>T | NCBI36 |
| NG_011806.1:g.49618T>A , LRG_553:g.49618T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367797.9:c.3176T>A MANE Select | ENSP00000356771.3:p.Phe1059Tyr | |
| ENST00000367796.3:c.3191T>A | ENSP00000356770.3:p.Phe1064Tyr | |
| ENST00000367797.7:c.3176T>A | ENSP00000356771.3:p.Phe1059Tyr | |
| NM_000130.4:c.3176T>A , LRG_553t1:c.3176T>A | NP_000121.2:p.Phe1059Tyr | |
| XM_017000660.2:c.2765T>A | XP_016856149.1:p.Phe922Tyr | |
| NM_000130.5:c.3176T>A MANE Select | NP_000121.2:p.Phe1059Tyr |