Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225583A>T , CM000668.2:g.3225583A>T | GRCh38 |
| NC_000006.11:g.3225817A>T , CM000668.1:g.3225817A>T | GRCh37 |
| NC_000006.10:g.3170816A>T | NCBI36 |
| NG_016715.1:g.7152T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.506T>A MANE Select | ENSP00000259818.6:p.Val169Asp | |
| ENST00000680070.1:n.1436T>A | ||
| ENST00000681707.1:n.1333T>A | ||
| ENST00000681757.1:n.811T>A | ||
| ENST00000259818.7:c.506T>A | ENSP00000259818.6:p.Val169Asp | |
| ENST00000473006.1:n.623T>A | ||
| NM_178012.4:c.506T>A | NP_821080.1:p.Val169Asp | |
| XM_011514571.1:c.290T>A | XP_011512873.1:p.Val97Asp | |
| NM_178012.5:c.506T>A MANE Select | NP_821080.1:p.Val169Asp |