HGVS | Genome Assembly |
---|---|
NC_000001.11:g.230702518T= , CM000663.2:g.230702518T= | GRCh38 |
NC_000001.10:g.230838264T= , CM000663.1:g.230838264T= | GRCh37 |
NC_000001.9:g.228904887T= | NCBI36 |
NG_008836.1:g.17073A= | |
NG_008836.2:g.17073A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000679738.1:c.*623A= | ENSP00000505063.1:n.*623A= | |
ENST00000679802.1:c.*1513A= | ENSP00000505184.1:n.*1513A= | |
ENST00000679854.1:n.6359A= | ||
ENST00000680041.1:c.*623A= | ENSP00000504866.1:n.*623A= | |
ENST00000680783.1:c.829+7477A= | ENSP00000506329.1:n.829+7477A= | |
ENST00000681347.1:n.4160A= | ||
ENST00000681514.1:c.*623A= | ENSP00000505963.1:n.*623A= | |
ENST00000681772.1:c.*1548A= | ENSP00000505829.1:n.*1548A= |