Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.99162881G>T , CM000669.2:g.99162881G>T | GRCh38 |
| NC_000007.13:g.98760504G>T , CM000669.1:g.98760504G>T | GRCh37 |
| NC_000007.12:g.98598440G>T | NCBI36 |
| NG_051213.1:g.61537C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_017012211.1:c.1545+15039C>A | XP_016867700.1:n.1545+15039C>A |