Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130452225C= , CM000671.2:g.130452225C= | GRCh38 |
| NC_000009.11:g.133327612C= , CM000671.1:g.133327612C= | GRCh37 |
| NC_000009.10:g.132317433C= | NCBI36 |
| NG_011542.1:g.12519C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_054012.4:c.-4C= MANE Select | NP_446464.1:n.-4C= |
| ENST00000352480.10:c.-4C= MANE Select | ENSP00000253004.6:n.-4C= |
| NM_000050.4:c.-4C= | NP_000041.2:n.-4C= |
| NM_054012.3:c.-4C= | NP_446464.1:n.-4C= |
| ENST00000352480.9:c.-4C= | ENSP00000253004.6:n.-4C= |
| ENST00000372393.7:c.-4C= | ENSP00000361469.2:n.-4C= |
| ENST00000372394.5:c.-4C= | ENSP00000361471.1:n.-4C= |
| ENST00000422569.5:c.-4C= | ENSP00000394212.1:n.-4C= |
| ENST00000443588.1:c.-4C= | ENSP00000397785.1:n.-4C= |
| XM_005272200.2:c.-4C= | XP_005272257.1:n.-4C= |
| XM_005272200.3:c.-4C= | XP_005272257.1:n.-4C= |
| XM_011518705.1:c.111C= | XP_011517007.1:p.Asp37= |
| XM_011518705.2:c.111C= | XP_011517007.1:p.Asp37= |
| XM_017014729.1:c.93C= | XP_016870218.1:p.Asp31= |