Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47322922C= , CM000672.2:g.47322922C= | GRCh38 |
| NC_000010.10:g.48416440G= , CM000672.1:g.48416440G= | GRCh37 |
| NC_000010.9:g.48036446G= | NCBI36 |
| NG_033916.1:g.5433C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000581492.3:c.254C= MANE Select | ENSP00000463051.1:p.Pro85= | |
| ENST00000581492.2:c.254C= | ENSP00000463051.1:p.Pro85= | |
| NM_016204.2:c.254C= | NP_057288.1:p.Pro85= | |
| XM_006717761.2:c.254C= | XP_006717824.1:p.Pro85= | |
| NM_016204.3:c.254C= | NP_057288.1:p.Pro85= | |
| NM_016204.4:c.254C= MANE Select | NP_057288.1:p.Pro85= |