HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039979G= , CM000663.2:g.55039979G= | GRCh38 |
NC_000001.10:g.55505652G= , CM000663.1:g.55505652G= | GRCh37 |
NC_000001.9:g.55278240G= | NCBI36 |
NG_009061.1:g.5433G= , LRG_275:g.5433G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000673913.2:c.142G= | ENSP00000501161.2:p.Glu48= | |
ENST00000710286.1:c.499G= | ENSP00000518176.1:p.Glu167= | |
ENST00000673726.1:c.142G= | ENSP00000501004.1:p.Glu48= | |
ENST00000302118.5:c.142G= MANE Select | ENSP00000303208.5:p.Glu48= | |
NM_174936.3:c.142G= , LRG_275t1:c.142G= | NP_777596.2:p.Glu48= | |
NM_174936.4:c.142G= MANE Select | NP_777596.2:p.Glu48= |