Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532522G>A , CM000665.2:g.129532522G>A | GRCh38 |
| NC_000003.11:g.129251365G>A , CM000665.1:g.129251365G>A | GRCh37 |
| NC_000003.10:g.130734055G>A | NCBI36 |
| NG_009115.1:g.8884G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000539.3:c.697-11G>A MANE Select | NP_000530.1:n.697-11G>A |
| ENST00000296271.4:c.697-11G>A MANE Select | ENSP00000296271.3:n.697-11G>A |
| ENST00000296271.3:c.697-11G>A | ENSP00000296271.3:n.697-11G>A |