| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99322775T= , CM000666.2:g.99322775T= | GRCh38 |
| NC_000004.11:g.100243932T= , CM000666.1:g.100243932T= | GRCh37 |
| NC_000004.10:g.100462955T= | NCBI36 |
| NG_011435.1:g.3641A= |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000639454.1:c.19-3889A= | ENSP00000491622.1:n.19-3889A= |