HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106940566T>A , CM000685.2:g.106940566T>A | GRCh38 |
NC_000023.10:g.106183796T>A , CM000685.1:g.106183796T>A | GRCh37 |
NC_000023.9:g.106070452T>A | NCBI36 |
NG_016392.1:g.64679A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000604604.1:c.111+52664A>T | ||
XM_005262190.3:c.*913A>T | XP_005262247.1:n.*913A>T | |
XM_006724691.2:c.*913A>T | XP_006724754.1:n.*913A>T | |
XM_011531027.2:c.*913A>T | XP_011529329.1:n.*913A>T | |
XM_017029844.1:c.*986A>T | XP_016885333.1:n.*986A>T |