Canonical Allele Identifier: CA2237371868

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889207G= , CM000678.2:g.81889207G=	GRCh38
NC_000016.9:g.81922812G= , CM000678.1:g.81922812G=	GRCh37
NC_000016.8:g.80480313G=	NCBI36
NG_032019.2:g.155111G= , LRG_376:g.155111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.801G=	ENSP00000455533.2:p.Glu267=
ENST00000697561.1:c.*230G=	ENSP00000513337.1:n.*230G=
ENST00000697562.1:c.801G=	ENSP00000513338.1:p.Glu267=
ENST00000697563.1:c.*647G=	ENSP00000513339.1:n.*647G=
ENST00000697564.1:c.684G=	ENSP00000513340.1:p.Glu228=
ENST00000697565.1:n.741G=
ENST00000697581.1:c.*795G=	ENSP00000513346.1:n.*795G=
ENST00000697582.1:c.801G=	ENSP00000513347.1:p.Glu267=
ENST00000697583.1:c.600G=	ENSP00000513349.1:p.Glu200=
ENST00000697584.1:c.600G=	ENSP00000513350.1:p.Glu200=
ENST00000697585.1:c.600G=	ENSP00000513351.1:p.Glu200=
ENST00000697586.1:c.600G=	ENSP00000513352.1:p.Glu200=
ENST00000697587.1:c.600G=	ENSP00000513353.1:p.Glu200=
ENST00000564138.6:c.801G= MANE Select	ENSP00000482457.1:p.Glu267=
ENST00000359376.7:c.801G=	ENSP00000352336.4:p.Glu267=
ENST00000563193.1:c.109G=
ENST00000564138.5:c.801G=	ENSP00000482457.1:p.Glu267=
ENST00000567980.5:n.1045G=
NM_002661.4:c.801G=	NP_002652.2:p.Glu267=
XM_011523108.1:c.915G=	XP_011521410.1:p.Glu305=
NM_002661.5:c.801G= MANE Select	NP_002652.2:p.Glu267=