HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12720397G= , CM000674.2:g.12720397G= | GRCh38 |
NC_000012.11:g.12873331G= , CM000674.1:g.12873331G= | GRCh37 |
NC_000012.10:g.12764598G= | NCBI36 |
NG_016341.1:g.8030G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.*1451G= | ENSP00000507272.1:n.*1451G= | |
ENST00000682620.1:n.1761-639G= | ||
ENST00000684771.1:n.715-639G= | ||
ENST00000228872.9:c.*9-639G= MANE Select | ENSP00000228872.4:n.*9-639G= | |
ENST00000228872.8:c.*9-639G= | ENSP00000228872.4:n.*9-639G= | |
ENST00000396340.1:c.476-668G= | ENSP00000379629.1:n.476-668G= | |
ENST00000442489.1:c.324-639G= | ENSP00000407597.1:n.324-639G= | |
ENST00000477087.1:n.285-639G= | ||
NM_004064.4:c.*9-639G= | NP_004055.1:n.*9-639G= | |
NM_004064.5:c.*9-639G= MANE Select | NP_004055.1:n.*9-639G= |