Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33068729A>C , CM000668.2:g.33068729A>C | GRCh38 |
| NC_000006.11:g.33036506A>C , CM000668.1:g.33036506A>C | GRCh37 |
| NC_000006.10:g.33144484A>C | NCBI36 |
| NG_033241.1:g.17050T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000692443.1:c.704T>G MANE Select | ENSP00000509163.1:p.Val235Gly | |
| ENST00000419277.5:c.704T>G | ENSP00000393566.1:p.Val235Gly | |
| ENST00000437811.1:c.306T>G | ||
| ENST00000479107.1:n.1303T>G | ||
| NM_001242524.1:c.704T>G | NP_001229453.1:p.Val235Gly | |
| NM_001242525.1:c.704T>G | NP_001229454.1:p.Val235Gly | |
| NM_033554.3:c.704T>G | NP_291032.2:p.Val235Gly | |
| XM_011514559.1:c.628+290T>G | XP_011512861.1:n.628+290T>G | |
| NM_001242524.2:c.704T>G | NP_001229453.1:p.Val235Gly | |
| NM_001242525.2:c.704T>G | NP_001229454.1:p.Val235Gly |