Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129531083T= , CM000665.2:g.129531083T= | GRCh38 |
| NC_000003.11:g.129249926T= , CM000665.1:g.129249926T= | GRCh37 |
| NC_000003.10:g.130732616T= | NCBI36 |
| NG_009115.1:g.7445T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.530+39T= MANE Select | ENSP00000296271.3:n.530+39T= | |
| ENST00000296271.3:c.530+39T= | ENSP00000296271.3:n.530+39T= | |
| NM_000539.3:c.530+39T= MANE Select | NP_000530.1:n.530+39T= |