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