Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92637495T>G , CM000672.2:g.92637495T>G | GRCh38 |
| NC_000010.10:g.94397252T>G , CM000672.1:g.94397252T>G | GRCh37 |
| NC_000010.9:g.94387232T>G | NCBI36 |
| NG_032580.1:g.49428T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2110T>G MANE Select | ENSP00000260731.3:p.Cys704Gly | |
| ENST00000676621.1:c.*628T>G | ENSP00000503639.1:n.*628T>G | |
| ENST00000676647.1:c.1903T>G | ENSP00000503394.1:p.Cys635Gly | |
| ENST00000676757.1:c.1903T>G | ENSP00000504289.1:p.Cys635Gly | |
| ENST00000677720.1:c.*84T>G | ENSP00000504840.1:n.*84T>G | |
| ENST00000260731.4:c.2110T>G | ENSP00000260731.3:p.Cys704Gly | |
| NM_004523.3:c.2110T>G | NP_004514.2:p.Cys704Gly | |
| NM_004523.4:c.2110T>G MANE Select | NP_004514.2:p.Cys704Gly |