Canonical Allele Identifier: CA2237371835

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889179G= , CM000678.2:g.81889179G=	GRCh38
NC_000016.9:g.81922784G= , CM000678.1:g.81922784G=	GRCh37
NC_000016.8:g.80480285G=	NCBI36
NG_032019.2:g.155083G= , LRG_376:g.155083G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.773G=	ENSP00000455533.2:p.Trp258=
ENST00000697561.1:c.*202G=	ENSP00000513337.1:n.*202G=
ENST00000697562.1:c.773G=	ENSP00000513338.1:p.Trp258=
ENST00000697563.1:c.*619G=	ENSP00000513339.1:n.*619G=
ENST00000697564.1:c.656G=	ENSP00000513340.1:p.Trp219=
ENST00000697565.1:n.713G=
ENST00000697581.1:c.*767G=	ENSP00000513346.1:n.*767G=
ENST00000697582.1:c.773G=	ENSP00000513347.1:p.Trp258=
ENST00000697583.1:c.572G=	ENSP00000513349.1:p.Trp191=
ENST00000697584.1:c.572G=	ENSP00000513350.1:p.Trp191=
ENST00000697585.1:c.572G=	ENSP00000513351.1:p.Trp191=
ENST00000697586.1:c.572G=	ENSP00000513352.1:p.Trp191=
ENST00000697587.1:c.572G=	ENSP00000513353.1:p.Trp191=
ENST00000564138.6:c.773G= MANE Select	ENSP00000482457.1:p.Trp258=
ENST00000359376.7:c.773G=	ENSP00000352336.4:p.Trp258=
ENST00000563193.1:c.81G=
ENST00000564138.5:c.773G=	ENSP00000482457.1:p.Trp258=
ENST00000567980.5:n.1017G=
NM_002661.4:c.773G=	NP_002652.2:p.Trp258=
XM_011523108.1:c.887G=	XP_011521410.1:p.Trp296=
NM_002661.5:c.773G= MANE Select	NP_002652.2:p.Trp258=