HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12718273C= , CM000674.2:g.12718273C= | GRCh38 |
NC_000012.11:g.12871207C= , CM000674.1:g.12871207C= | GRCh37 |
NC_000012.10:g.12762474C= | NCBI36 |
NG_016341.1:g.5906C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614874.2:c.434C= | ENSP00000507272.1:p.Ala145= | |
ENST00000682620.1:n.1631-552C= | ||
ENST00000684771.1:n.585-552C= | ||
ENST00000228872.9:c.434C= MANE Select | ENSP00000228872.4:p.Ala145= | |
ENST00000228872.8:c.434C= | ENSP00000228872.4:p.Ala145= | |
ENST00000396340.1:c.434C= | ENSP00000379629.1:p.Ala145= | |
ENST00000442489.1:c.193+220C= | ENSP00000407597.1:n.193+220C= | |
ENST00000477087.1:n.155-552C= | ||
NM_004064.4:c.434C= | NP_004055.1:p.Ala145= | |
NM_004064.5:c.434C= MANE Select | NP_004055.1:p.Ala145= |