Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420762C>A , CM000666.2:g.99420762C>A | GRCh38 |
| NC_000004.11:g.100341919C>A , CM000666.1:g.100341919C>A | GRCh37 |
| NC_000004.10:g.100560942C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.596G>T MANE Select | ENSP00000414254.2:p.Gly199Val | |
| ENST00000209665.8:c.632G>T | ENSP00000209665.4:p.Gly211Val | |
| ENST00000437033.6:c.596G>T | ENSP00000414254.2:p.Gly199Val | |
| ENST00000476959.5:c.656G>T | ENSP00000420269.1:p.Gly219Val | |
| ENST00000482593.5:c.425G>T | ENSP00000420613.1:p.Gly142Val | |
| NM_000673.4:c.632G>T | NP_000664.2:p.Gly211Val | |
| NM_001166504.1:c.656G>T | NP_001159976.1:p.Gly219Val | |
| NM_000673.7:c.596G>T MANE Select | NP_000664.3:p.Gly199Val | |
| NM_001166504.2:c.656G>T | NP_001159976.1:p.Gly219Val |