HGVS | Genome Assembly |
---|---|
NC_000022.11:g.21658391C>G , CM000684.2:g.21658391C>G | GRCh38 |
NC_000022.10:g.22012680C>G , CM000684.1:g.22012680C>G | GRCh37 |
NC_000022.9:g.20342680C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000641967.1:n.286+2C>G | ||
ENST00000498589.1:n.468C>G | ||
XM_017029165.1:c.603C>G | XP_016884654.1:p.Gly201= | |
NR_169729.1:n.1203C>G | ||
NR_169730.1:n.1106C>G | ||
NR_169731.1:n.432-2446C>G | ||
NR_169732.1:n.257C>G | ||
NR_169733.1:n.315C>G | ||
NR_169734.1:n.339C>G |