| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.13488772C>A , CM000674.2:g.13488772C>A | GRCh38 |
| NC_000012.11:g.13641706C>A , CM000674.1:g.13641706C>A | GRCh37 |
| NC_000012.10:g.13532973C>A | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000637214.1:c.70-50761G>T | ENSP00000489997.1:n.70-50761G>T |