Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912311C= , CM000674.2:g.4912311C= | GRCh38 |
| NC_000012.11:g.5021477C= , CM000674.1:g.5021477C= | GRCh37 |
| NC_000012.10:g.4891738C= | NCBI36 |
| NG_011815.1:g.7405C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.933C= MANE Select | ENSP00000371985.3:p.Gly311= | |
| ENST00000543874.3:n.105+1839C= | ||
| ENST00000639306.1:c.771C= | ENSP00000492506.1:p.Gly257= | |
| ENST00000639680.1:c.76+45C= | ||
| ENST00000382545.3:c.933C= | ENSP00000371985.3:p.Gly311= | |
| ENST00000541095.1:n.105+1839C= | ||
| ENST00000543874.2:n.96+1839C= | ||
| NM_000217.2:c.933C= | NP_000208.2:p.Gly311= | |
| NM_000217.3:c.933C= MANE Select | NP_000208.2:p.Gly311= |