HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039916G>A , CM000663.2:g.55039916G>A | GRCh38 |
NC_000001.10:g.55505589G>A , CM000663.1:g.55505589G>A | GRCh37 |
NC_000001.9:g.55278177G>A | NCBI36 |
NG_009061.1:g.5370G>A , LRG_275:g.5370G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.79G>A | ENSP00000501161.2:p.Gly27Ser | |
ENST00000710286.1:c.436G>A | ENSP00000518176.1:p.Gly146Ser | |
ENST00000673726.1:c.79G>A | ENSP00000501004.1:p.Gly27Ser | |
ENST00000302118.5:c.79G>A MANE Select | ENSP00000303208.5:p.Gly27Ser | |
NM_174936.3:c.79G>A , LRG_275t1:c.79G>A | NP_777596.2:p.Gly27Ser | |
NM_174936.4:c.79G>A MANE Select | NP_777596.2:p.Gly27Ser |