HGVS | Genome Assembly |
---|---|
NC_000017.11:g.49363186T>C , CM000679.2:g.49363186T>C | GRCh38 |
NC_000017.10:g.47440548T>C , CM000679.1:g.47440548T>C | GRCh37 |
NC_000017.9:g.44795547T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_110882.1:n.136+669T>C | ||
NR_110883.1:n.31-1093T>C | ||
NR_110884.1:n.58-1093T>C |