Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749576C= , CM000677.2:g.74749576C= | GRCh38 |
| NC_000015.9:g.75041917C= , CM000677.1:g.75041917C= | GRCh37 |
| NC_000015.8:g.72828970C= | NCBI36 |
| NG_008431.1:g.32035C= | |
| NG_008431.2:g.32035C= | |
| NG_061543.1:g.5732C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000761.5:c.-9-154C= MANE Select | NP_000752.2:n.-9-154C= |
| ENST00000343932.5:c.-9-154C= MANE Select | ENSP00000342007.4:n.-9-154C= |
| NM_000761.4:c.-9-154C= | NP_000752.2:n.-9-154C= |
| ENST00000343932.4:c.-9-154C= | ENSP00000342007.4:n.-9-154C= |