HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42132714G>C , CM000684.2:g.42132714G>C | GRCh38 |
NC_000022.10:g.42528721G>C , CM000684.1:g.42528721G>C | GRCh37 |
NC_000022.9:g.40858665G>C | NCBI36 |
NG_008376.3:g.2278C>G | |
NG_008376.4:g.3097C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000417586.1:n.172G>C | ||
XM_011529967.1:c.-1045-878C>G | XP_011528269.1:n.-1045-878C>G |