HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42130967C= , CM000684.2:g.42130967C= | GRCh38 |
NC_000022.10:g.42526969C= , CM000684.1:g.42526969C= | GRCh37 |
NC_000022.9:g.40856913C= | NCBI36 |
NG_008376.3:g.4025G= | |
NG_008376.4:g.4844G= |
HGVS | Amino-acid Change |
---|---|
XM_011529966.1:c.-176G= | XP_011528268.1:n.-176G= |
XM_011529967.1:c.-176G= | XP_011528269.1:n.-176G= |
XM_011529968.1:c.-176G= | XP_011528270.1:n.-176G= |
XM_011529969.1:c.37+330G= | XP_011528271.1:n.37+330G= |
XM_011529970.1:c.-176G= | XP_011528272.1:n.-176G= |
XM_011529971.1:c.37+330G= | XP_011528273.1:n.37+330G= |
XM_011529972.1:c.-176G= | XP_011528274.1:n.-176G= |
XR_002958749.1:n.275+279C= | |
XR_430455.2:n.328+279C= |