Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129531048A>T , CM000665.2:g.129531048A>T | GRCh38 |
| NC_000003.11:g.129249891A>T , CM000665.1:g.129249891A>T | GRCh37 |
| NC_000003.10:g.130732581A>T | NCBI36 |
| NG_009115.1:g.7410A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.530+4A>T MANE Select | ENSP00000296271.3:n.530+4A>T | |
| ENST00000296271.3:c.530+4A>T | ENSP00000296271.3:n.530+4A>T | |
| NM_000539.3:c.530+4A>T MANE Select | NP_000530.1:n.530+4A>T |