HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717948G>T , CM000674.2:g.12717948G>T | GRCh38 |
NC_000012.11:g.12870882G>T , CM000674.1:g.12870882G>T | GRCh37 |
NC_000012.10:g.12762149G>T | NCBI36 |
NG_016341.1:g.5581G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.109G>T | ENSP00000507272.1:p.Asp37Tyr | |
ENST00000682620.1:n.1631-877G>T | ||
ENST00000684771.1:n.585-877G>T | ||
ENST00000228872.9:c.109G>T MANE Select | ENSP00000228872.4:p.Asp37Tyr | |
ENST00000228872.8:c.109G>T | ENSP00000228872.4:p.Asp37Tyr | |
ENST00000396340.1:c.109G>T | ENSP00000379629.1:p.Asp37Tyr | |
ENST00000442489.1:c.88G>T | ENSP00000407597.1:p.Asp30Tyr | |
ENST00000477087.1:n.155-877G>T | ||
NM_004064.4:c.109G>T | NP_004055.1:p.Asp37Tyr | |
NM_004064.5:c.109G>T MANE Select | NP_004055.1:p.Asp37Tyr |