Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165069022T= , CM000665.2:g.165069022T= | GRCh38 |
| NC_000003.11:g.164786810T= , CM000665.1:g.164786810T= | GRCh37 |
| NC_000003.10:g.166269504T= | NCBI36 |
| NG_017043.1:g.14474A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264382.8:c.373+56A= MANE Select | ENSP00000264382.3:n.373+56A= | |
| ENST00000264382.7:c.373+56A= | ENSP00000264382.3:n.373+56A= | |
| ENST00000476593.1:c.*248+56A= | ENSP00000419450.1:n.*248+56A= | |
| NM_001041.3:c.373+56A= | NP_001032.2:n.373+56A= | |
| XM_011513078.1:c.274+56A= | XP_011511380.1:n.274+56A= | |
| XM_011513078.2:c.274+56A= | XP_011511380.1:n.274+56A= | |
| NM_001041.4:c.373+56A= MANE Select | NP_001032.2:n.373+56A= |