HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039938A>G , CM000663.2:g.55039938A>G | GRCh38 |
NC_000001.10:g.55505611A>G , CM000663.1:g.55505611A>G | GRCh37 |
NC_000001.9:g.55278199A>G | NCBI36 |
NG_009061.1:g.5392A>G , LRG_275:g.5392A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.101A>G | ENSP00000501161.2:p.Glu34Gly | |
ENST00000710286.1:c.458A>G | ENSP00000518176.1:p.Glu153Gly | |
ENST00000673726.1:c.101A>G | ENSP00000501004.1:p.Glu34Gly | |
ENST00000302118.5:c.101A>G MANE Select | ENSP00000303208.5:p.Glu34Gly | |
NM_174936.3:c.101A>G , LRG_275t1:c.101A>G | NP_777596.2:p.Glu34Gly | |
NM_174936.4:c.101A>G MANE Select | NP_777596.2:p.Glu34Gly |