Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129533606A>G , CM000665.2:g.129533606A>G | GRCh38 |
| NC_000003.11:g.129252449A>G , CM000665.1:g.129252449A>G | GRCh37 |
| NC_000003.10:g.130735139A>G | NCBI36 |
| NG_009115.1:g.9968A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000539.3:c.937-2A>G MANE Select | NP_000530.1:n.937-2A>G |
| ENST00000296271.4:c.937-2A>G MANE Select | ENSP00000296271.3:n.937-2A>G |
| ENST00000296271.3:c.937-2A>G | ENSP00000296271.3:n.937-2A>G |