HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3154768A>C , CM000668.2:g.3154768A>C | GRCh38 |
NC_000006.11:g.3155002A>C , CM000668.1:g.3155002A>C | GRCh37 |
NC_000006.10:g.3100001A>C | NCBI36 |
NG_042223.1:g.7782T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333628.4:c.433T>G MANE Select | ENSP00000369703.2:p.Ser145Ala | |
ENST00000679400.1:n.489T>G | ||
ENST00000679907.1:n.821T>G | ||
ENST00000680036.1:n.1215T>G | ||
ENST00000680967.1:n.1523T>G | ||
ENST00000333628.3:c.433T>G | ENSP00000369703.2:p.Ser145Ala | |
ENST00000489942.1:n.628T>G | ||
NM_001069.2:c.433T>G | NP_001060.1:p.Ser145Ala | |
NM_001310315.1:c.178T>G | NP_001297244.1:p.Ser60Ala | |
NM_001069.3:c.433T>G MANE Select | NP_001060.1:p.Ser145Ala | |
NM_001310315.2:c.178T>G | NP_001297244.1:p.Ser60Ala |