Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17024041A= , CM000663.2:g.17024041A= | GRCh38 |
| NC_000001.10:g.17350536A= , CM000663.1:g.17350536A= | GRCh37 |
| NC_000001.9:g.17223123A= | NCBI36 |
| NG_012340.1:g.35130T= , LRG_316:g.35130T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.403T= | ENSP00000481376.2:p.Cys135= | |
| ENST00000491274.6:c.532T= | ENSP00000480482.2:p.Cys178= | |
| ENST00000375499.8:c.574T= MANE Select | ENSP00000364649.3:p.Cys192= | |
| ENST00000375499.7:c.574T= | ENSP00000364649.3:p.Cys192= | |
| ENST00000485515.5:n.508T= | ||
| ENST00000491274.5:c.532T= | ENSP00000480482.1:p.Cys178= | |
| NM_003000.2:c.574T= , LRG_316t1:c.574T= | NP_002991.2:p.Cys192= | |
| NM_003000.3:c.574T= MANE Select | NP_002991.2:p.Cys192= |