Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186849003T>C , CM000665.2:g.186849003T>C | GRCh38 |
| NC_000003.11:g.186566792T>C , CM000665.1:g.186566792T>C | GRCh37 |
| NC_000003.10:g.188049486T>C | NCBI36 |
| NG_021140.1:g.11330T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320741.7:c.-8-4048T>C MANE Select | ENSP00000320709.2:n.-8-4048T>C | |
| ENST00000320741.6:c.-8-4048T>C | ENSP00000320709.2:n.-8-4048T>C | |
| ENST00000444204.2:c.-9+3396T>C | ENSP00000389814.2:n.-9+3396T>C | |
| NM_001177800.1:c.-9+3396T>C | NP_001171271.1:n.-9+3396T>C | |
| NM_004797.3:c.-8-4048T>C | NP_004788.1:n.-8-4048T>C | |
| XM_011513324.1:c.-124-2103T>C | XP_011511626.1:n.-124-2103T>C | |
| NM_004797.4:c.-8-4048T>C MANE Select | NP_004788.1:n.-8-4048T>C | |
| NM_001177800.2:c.-9+3396T>C | NP_001171271.1:n.-9+3396T>C |