HGVS | Genome Assembly |
---|---|
NC_000003.12:g.180659449T= , CM000665.2:g.180659449T= | GRCh38 |
NC_000003.11:g.180377237T= , CM000665.1:g.180377237T= | GRCh37 |
NC_000003.10:g.181859931T= | NCBI36 |
NG_029581.1:g.25047A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000476379.6:c.738+3A= MANE Select | ENSP00000417960.2:n.738+3A= | |
ENST00000650641.1:n.817+3A= | ||
ENST00000650889.1:n.910+3A= | ||
ENST00000651046.1:c.738+3A= | ENSP00000499175.1:n.738+3A= | |
ENST00000651818.1:n.880+3A= | ||
ENST00000652024.1:n.829+3A= | ||
ENST00000652408.1:n.875+3A= | ||
ENST00000442201.6:c.738+3A= | ENSP00000405708.2:n.738+3A= | |
ENST00000476379.5:c.738+3A= | ENSP00000417960.1:n.738+3A= | |
NM_181426.1:c.738+3A= | NP_852091.1:n.738+3A= | |
NM_181426.2:c.738+3A= MANE Select | NP_852091.1:n.738+3A= |