HGVS | Genome Assembly |
---|---|
NC_000015.10:g.96287298T>C , CM000677.2:g.96287298T>C | GRCh38 |
NC_000015.9:g.96830527T>C , CM000677.1:g.96830527T>C | GRCh37 |
NC_000015.8:g.94631531T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_102743.1:n.409+1366A>G | ||
NR_125738.1:n.317+3332A>G |