| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.100142995C>A , CM000664.2:g.100142995C>A | GRCh38 |
| NC_000002.11:g.100759457C>A , CM000664.1:g.100759457C>A | GRCh37 |
| NC_000002.10:g.100125889C>A | NCBI36 |
| NG_052835.1:g.4589G>T |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000672999.1:n.288-400G>T |