Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129529095G>A , CM000665.2:g.129529095G>A | GRCh38 |
| NC_000003.11:g.129247938G>A , CM000665.1:g.129247938G>A | GRCh37 |
| NC_000003.10:g.130730628G>A | NCBI36 |
| NG_009115.1:g.5457G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.361+1G>A MANE Select | ENSP00000296271.3:n.361+1G>A | |
| ENST00000296271.3:c.361+1G>A | ENSP00000296271.3:n.361+1G>A | |
| NM_000539.3:c.361+1G>A MANE Select | NP_000530.1:n.361+1G>A |