| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.715725T= , CM000679.2:g.715725T= | GRCh38 |
| NC_000017.10:g.618965T= , CM000679.1:g.618965T= | GRCh37 |
| NC_000017.9:g.565715T= | NCBI36 |
| NG_034190.1:g.4132A= |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000576019.5:c.-282-5112A= | ENSP00000461429.1:n.-282-5112A= |
| ENST00000680704.1:c.-282-5112A= | ENSP00000506453.1:n.-282-5112A= |