HGVS | Genome Assembly |
---|---|
NC_000010.11:g.92645441A>G , CM000672.2:g.92645441A>G | GRCh38 |
NC_000010.10:g.94405198A>G , CM000672.1:g.94405198A>G | GRCh37 |
NC_000010.9:g.94395178A>G | NCBI36 |
NG_032580.1:g.57374A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260731.5:c.2346A>G MANE Select | ENSP00000260731.3:p.Glu782= | |
ENST00000676621.1:c.*864A>G | ENSP00000503639.1:n.*864A>G | |
ENST00000676647.1:c.2139A>G | ENSP00000503394.1:p.Glu713= | |
ENST00000676757.1:c.2139A>G | ENSP00000504289.1:p.Glu713= | |
ENST00000677720.1:c.*320A>G | ENSP00000504840.1:n.*320A>G | |
ENST00000260731.4:c.2346A>G | ENSP00000260731.3:p.Glu782= | |
NM_004523.3:c.2346A>G | NP_004514.2:p.Glu782= | |
NM_004523.4:c.2346A>G MANE Select | NP_004514.2:p.Glu782= |