HGVS | Genome Assembly |
---|---|
NC_000017.11:g.49363116T>C , CM000679.2:g.49363116T>C | GRCh38 |
NC_000017.10:g.47440478T>C , CM000679.1:g.47440478T>C | GRCh37 |
NC_000017.9:g.44795477T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_110882.1:n.136+599T>C | ||
NR_110883.1:n.31-1163T>C | ||
NR_110884.1:n.58-1163T>C |