HGVS | Genome Assembly |
---|---|
NC_000017.11:g.69854776T>C , CM000679.2:g.69854776T>C | GRCh38 |
NC_000017.10:g.67850917T>C , CM000679.1:g.67850917T>C | GRCh37 |
NC_000017.9:g.65362512T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_109971.1:n.363+9290T>C | ||
NR_109972.1:n.363+9290T>C |