Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852860G= , CM000674.2:g.102852860G= | GRCh38 |
| NC_000012.11:g.103246638G= , CM000674.1:g.103246638G= | GRCh37 |
| NC_000012.10:g.101770768G= | NCBI36 |
| NG_008690.1:g.69743C= | |
| NG_008690.2:g.110551C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.797C= MANE Select | ENSP00000448059.1:p.Thr266= | |
| ENST00000307000.7:c.782C= | ENSP00000303500.2:p.Thr261= | |
| ENST00000549247.6:n.556C= | ||
| ENST00000553106.5:c.797C= | ENSP00000448059.1:p.Thr266= | |
| NM_000277.1:c.797C= | NP_000268.1:p.Thr266= | |
| XM_011538422.1:c.797C= | XP_011536724.1:p.Thr266= | |
| NM_000277.2:c.797C= | NP_000268.1:p.Thr266= | |
| NM_001354304.1:c.797C= | NP_001341233.1:p.Thr266= | |
| NM_000277.3:c.797C= MANE Select | NP_000268.1:p.Thr266= | |
| NM_001354304.2:c.797C= | NP_001341233.1:p.Thr266= |