Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10122041C>A , CM000665.2:g.10122041C>A | GRCh38 |
| NC_000003.11:g.10163725C>A , CM000665.1:g.10163725C>A | GRCh37 |
| NC_000003.10:g.10138725C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018462.5:c.119-3585C>A MANE Select | NP_060932.2:n.119-3585C>A |
| ENST00000530758.2:c.119-3585C>A MANE Select | ENSP00000432472.1:n.119-3585C>A |
| NM_018462.4:c.119-3585C>A | NP_060932.2:n.119-3585C>A |
| ENST00000530758.1:c.119-3585C>A | ENSP00000432472.1:n.119-3585C>A |