Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4631983G>C , CM000679.2:g.4631983G>C | GRCh38 |
| NC_000017.10:g.4535278G>C , CM000679.1:g.4535278G>C | GRCh37 |
| NC_000017.9:g.4482027G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293761.8:c.1715C>G MANE Select | ENSP00000293761.3:p.Thr572Arg | |
| ENST00000570836.6:c.1715C>G | ENSP00000458832.1:p.Thr572Arg | |
| ENST00000293761.7:c.1715C>G | ENSP00000293761.3:p.Thr572Arg | |
| ENST00000570836.5:c.1715C>G | ENSP00000458832.1:p.Thr572Arg | |
| ENST00000574640.1:c.1598C>G | ENSP00000460483.1:p.Thr533Arg | |
| NM_001140.3:c.1715C>G | NP_001131.3:p.Thr572Arg | |
| NM_001140.4:c.1715C>G | NP_001131.3:p.Thr572Arg | |
| NM_001140.5:c.1715C>G MANE Select | NP_001131.3:p.Thr572Arg |