HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717817G= , CM000674.2:g.12717817G= | GRCh38 |
NC_000012.11:g.12870751G= , CM000674.1:g.12870751G= | GRCh37 |
NC_000012.10:g.12762018G= | NCBI36 |
NG_016341.1:g.5450G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.-23G= | ENSP00000507272.1:n.-23G= | |
ENST00000682620.1:n.1631-1008G= | ||
ENST00000684771.1:n.585-1008G= | ||
ENST00000228872.9:c.-23G= MANE Select | ENSP00000228872.4:n.-23G= | |
ENST00000228872.8:c.-23G= | ENSP00000228872.4:n.-23G= | |
ENST00000477087.1:n.155-1008G= | ||
NM_004064.4:c.-23G= | NP_004055.1:n.-23G= | |
NM_004064.5:c.-23G= MANE Select | NP_004055.1:n.-23G= |