HGVS | Genome Assembly |
---|---|
NC_000015.10:g.96287067T>C , CM000677.2:g.96287067T>C | GRCh38 |
NC_000015.9:g.96830296T>C , CM000677.1:g.96830296T>C | GRCh37 |
NC_000015.8:g.94631300T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_102743.1:n.409+1597A>G | ||
NR_125738.1:n.317+3563A>G |