HGVS | Genome Assembly |
---|---|
NC_000012.12:g.93585972C>G , CM000674.2:g.93585972C>G | GRCh38 |
NC_000012.11:g.93979748C>G , CM000674.1:g.93979748C>G | GRCh37 |
NC_000012.10:g.92503879C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_005269213.3:c.*213C>G | XP_005269270.2:n.*213C>G | |
XM_006719673.1:c.*213C>G | XP_006719736.1:n.*213C>G | |
XM_006719674.1:c.*213C>G | XP_006719737.1:n.*213C>G | |
XM_011538929.1:c.*213C>G | XP_011537231.1:n.*213C>G | |
XM_011538930.1:c.*213C>G | XP_011537232.1:n.*213C>G | |
XM_011538931.1:c.*213C>G | XP_011537233.1:n.*213C>G | |
XM_011538932.1:c.*213C>G | XP_011537234.1:n.*213C>G | |
XM_011538933.1:c.*213C>G | XP_011537235.1:n.*213C>G | |
XM_011538934.1:c.*213C>G | XP_011537236.1:n.*213C>G | |
XM_011538935.1:c.591+10799C>G | XP_011537237.1:n.591+10799C>G | |
XR_944810.1:n.1557C>G |