Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800257C= , CM000666.2:g.24800257C= | GRCh38 |
| NC_000004.11:g.24801879C= , CM000666.1:g.24801879C= | GRCh37 |
| NC_000004.10:g.24410977C= | NCBI36 |
| NG_012213.1:g.9795C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.*13C= MANE Select | ENSP00000371554.3:n.*13C= | |
| ENST00000382120.3:c.*13C= | ENSP00000371554.3:n.*13C= | |
| NM_003102.2:c.*13C= | NP_003093.2:n.*13C= | |
| XR_427488.1:n.926C= | ||
| NM_003102.3:c.*13C= | NP_003093.2:n.*13C= | |
| NM_003102.4:c.*13C= MANE Select | NP_003093.2:n.*13C= |