HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161521166T= , CM000663.2:g.161521166T= | GRCh38 |
NC_000001.10:g.161490956T= , CM000663.1:g.161490956T= | GRCh37 |
NC_000001.9:g.159757580T= | NCBI36 |
NG_012066.1:g.20752T= | |
NG_012066.2:g.20752T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467525.5:c.918+1453T= | ENSP00000476495.1:n.918+1453T= | |
ENST00000491841.1:n.425+1175T= | ||
XM_011509287.1:c.*23+1175T= | XP_011507589.1:n.*23+1175T= | |
XM_011509288.1:c.*23+1175T= | XP_011507590.1:n.*23+1175T= | |
XM_011509289.1:c.*23+1175T= | XP_011507591.1:n.*23+1175T= | |
XM_011509287.2:c.*23+1175T= | XP_011507589.1:n.*23+1175T= | |
XM_017000664.1:c.944-2124T= | XP_016856153.1:n.944-2124T= | |
XM_017000665.1:c.944-2124T= | XP_016856154.1:n.944-2124T= | |
XR_001737042.1:n.1171+1175T= |