Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33068748C>T , CM000668.2:g.33068748C>T | GRCh38 |
| NC_000006.11:g.33036525C>T , CM000668.1:g.33036525C>T | GRCh37 |
| NC_000006.10:g.33144503C>T | NCBI36 |
| NG_033241.1:g.17031G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000692443.1:c.685G>A MANE Select | ENSP00000509163.1:p.Gly229Ser | |
| ENST00000419277.5:c.685G>A | ENSP00000393566.1:p.Gly229Ser | |
| ENST00000437811.1:c.287G>A | ||
| ENST00000479107.1:n.1284G>A | ||
| NM_001242524.1:c.685G>A | NP_001229453.1:p.Gly229Ser | |
| NM_001242525.1:c.685G>A | NP_001229454.1:p.Gly229Ser | |
| NM_033554.3:c.685G>A | NP_291032.2:p.Gly229Ser | |
| XM_011514559.1:c.628+271G>A | XP_011512861.1:n.628+271G>A | |
| NM_001242524.2:c.685G>A | NP_001229453.1:p.Gly229Ser | |
| NM_001242525.2:c.685G>A | NP_001229454.1:p.Gly229Ser |