HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106940440C>A , CM000685.2:g.106940440C>A | GRCh38 |
NC_000023.10:g.106183670C>A , CM000685.1:g.106183670C>A | GRCh37 |
NC_000023.9:g.106070326C>A | NCBI36 |
NG_016392.1:g.64805G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000604604.1:c.111+52790G>T | ||
XM_005262190.3:c.*1039G>T | XP_005262247.1:n.*1039G>T | |
XM_006724691.2:c.*1039G>T | XP_006724754.1:n.*1039G>T | |
XM_011531027.2:c.*1039G>T | XP_011529329.1:n.*1039G>T | |
XM_017029844.1:c.*1112G>T | XP_016885333.1:n.*1112G>T |