| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99329262C= , CM000666.2:g.99329262C= | GRCh38 |
| NC_000004.11:g.100250419C= , CM000666.1:g.100250419C= | GRCh37 |
| NC_000004.10:g.100469442C= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000639454.1:c.19-10376G= | ENSP00000491622.1:n.19-10376G= |