Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74753234G= , CM000677.2:g.74753234G= | GRCh38 |
| NC_000015.9:g.75045575G= , CM000677.1:g.75045575G= | GRCh37 |
| NC_000015.8:g.72832628G= | NCBI36 |
| NG_008431.1:g.35693G= | |
| NG_008431.2:g.35693G= | |
| NG_061543.1:g.9390G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000761.5:c.1217G= MANE Select | NP_000752.2:p.Cys406= |
| ENST00000343932.5:c.1217G= MANE Select | ENSP00000342007.4:p.Cys406= |
| NM_000761.4:c.1217G= | NP_000752.2:p.Cys406= |
| ENST00000343932.4:c.1217G= | ENSP00000342007.4:p.Cys406= |