Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186849130T= , CM000665.2:g.186849130T= | GRCh38 |
| NC_000003.11:g.186566919T= , CM000665.1:g.186566919T= | GRCh37 |
| NC_000003.10:g.188049613T= | NCBI36 |
| NG_021140.1:g.11457T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320741.7:c.-8-3921T= MANE Select | ENSP00000320709.2:n.-8-3921T= | |
| ENST00000320741.6:c.-8-3921T= | ENSP00000320709.2:n.-8-3921T= | |
| ENST00000444204.2:c.-9+3523T= | ENSP00000389814.2:n.-9+3523T= | |
| NM_001177800.1:c.-9+3523T= | NP_001171271.1:n.-9+3523T= | |
| NM_004797.3:c.-8-3921T= | NP_004788.1:n.-8-3921T= | |
| XM_011513324.1:c.-124-1976T= | XP_011511626.1:n.-124-1976T= | |
| NM_004797.4:c.-8-3921T= MANE Select | NP_004788.1:n.-8-3921T= | |
| NM_001177800.2:c.-9+3523T= | NP_001171271.1:n.-9+3523T= |