Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529659T>G , CM000681.2:g.7529659T>G | GRCh38 |
| NC_000019.9:g.7594545T>G , CM000681.1:g.7594545T>G | GRCh37 |
| NC_000019.8:g.7500545T>G | NCBI36 |
| NG_013374.1:g.508T>G | |
| NG_015806.1:g.12050T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1306T>G MANE Select | ENSP00000264079.5:p.Tyr436Asp | |
| ENST00000264079.10:c.1306T>G | ENSP00000264079.5:p.Tyr436Asp | |
| ENST00000394321.9:n.1621T>G | ||
| ENST00000594692.1:n.302T>G | ||
| ENST00000595860.5:n.489T>G | ||
| ENST00000599334.1:c.183T>G | ||
| NM_020533.2:c.1306T>G | NP_065394.1:p.Tyr436Asp | |
| NM_020533.3:c.1306T>G MANE Select | NP_065394.1:p.Tyr436Asp |