HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42130979G>T , CM000684.2:g.42130979G>T | GRCh38 |
NC_000022.10:g.42526981G>T , CM000684.1:g.42526981G>T | GRCh37 |
NC_000022.9:g.40856925G>T | NCBI36 |
NG_008376.3:g.4013C>A | |
NG_008376.4:g.4832C>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011529966.1:c.-188C>A | XP_011528268.1:n.-188C>A | |
XM_011529967.1:c.-188C>A | XP_011528269.1:n.-188C>A | |
XM_011529968.1:c.-188C>A | XP_011528270.1:n.-188C>A | |
XM_011529969.1:c.37+318C>A | XP_011528271.1:n.37+318C>A | |
XM_011529970.1:c.-188C>A | XP_011528272.1:n.-188C>A | |
XM_011529971.1:c.37+318C>A | XP_011528273.1:n.37+318C>A | |
XM_011529972.1:c.-188C>A | XP_011528274.1:n.-188C>A | |
XR_430455.2:n.328+291G>T | ||
XR_002958749.1:n.275+291G>T |