HGVS | Genome Assembly |
---|---|
NC_000022.11:g.21658217C>G , CM000684.2:g.21658217C>G | GRCh38 |
NC_000022.10:g.22012506C>G , CM000684.1:g.22012506C>G | GRCh37 |
NC_000022.9:g.20342506C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000641967.1:n.163-49C>G | ||
ENST00000498589.1:n.343-49C>G | ||
XM_017029165.1:c.478-49C>G | XP_016884654.1:n.478-49C>G | |
NR_169729.1:n.1029C>G | ||
NR_169730.1:n.932C>G | ||
NR_169731.1:n.432-2620C>G | ||
NR_169732.1:n.132-49C>G | ||
NR_169733.1:n.214-73C>G | ||
NR_169734.1:n.214-49C>G |