Canonical Allele Identifier: CA2237372243

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889469C= , CM000678.2:g.81889469C=	GRCh38
NC_000016.9:g.81923074C= , CM000678.1:g.81923074C=	GRCh37
NC_000016.8:g.80480575C=	NCBI36
NG_032019.2:g.155373C= , LRG_376:g.155373C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+196C=	ENSP00000455533.2:n.867+196C=
ENST00000697561.1:c.*296+196C=	ENSP00000513337.1:n.*296+196C=
ENST00000697562.1:c.867+196C=	ENSP00000513338.1:n.867+196C=
ENST00000697563.1:c.*713+196C=	ENSP00000513339.1:n.*713+196C=
ENST00000697564.1:c.750+196C=	ENSP00000513340.1:n.750+196C=
ENST00000697565.1:n.807+196C=
ENST00000697581.1:c.*861+196C=	ENSP00000513346.1:n.*861+196C=
ENST00000697582.1:c.867+196C=	ENSP00000513347.1:n.867+196C=
ENST00000697583.1:c.666+196C=	ENSP00000513349.1:n.666+196C=
ENST00000697584.1:c.666+196C=	ENSP00000513350.1:n.666+196C=
ENST00000697585.1:c.666+196C=	ENSP00000513351.1:n.666+196C=
ENST00000697586.1:c.666+196C=	ENSP00000513352.1:n.666+196C=
ENST00000697587.1:c.666+196C=	ENSP00000513353.1:n.666+196C=
ENST00000564138.6:c.867+196C= MANE Select	ENSP00000482457.1:n.867+196C=
ENST00000359376.7:c.867+196C=	ENSP00000352336.4:n.867+196C=
ENST00000562605.5:n.61+70C=
ENST00000563193.1:c.175+196C=
ENST00000564138.5:c.867+196C=	ENSP00000482457.1:n.867+196C=
ENST00000567980.5:n.1111+196C=
NM_002661.4:c.867+196C=	NP_002652.2:n.867+196C=
XM_011523108.1:c.981+196C=	XP_011521410.1:n.981+196C=
NM_002661.5:c.867+196C= MANE Select	NP_002652.2:n.867+196C=