Canonical Allele Identifier: CA2237371923

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889233C= , CM000678.2:g.81889233C=	GRCh38
NC_000016.9:g.81922838C= , CM000678.1:g.81922838C=	GRCh37
NC_000016.8:g.80480339C=	NCBI36
NG_032019.2:g.155137C= , LRG_376:g.155137C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.827C=	ENSP00000455533.2:p.Thr276=
ENST00000697561.1:c.*256C=	ENSP00000513337.1:n.*256C=
ENST00000697562.1:c.827C=	ENSP00000513338.1:p.Thr276=
ENST00000697563.1:c.*673C=	ENSP00000513339.1:n.*673C=
ENST00000697564.1:c.710C=	ENSP00000513340.1:p.Thr237=
ENST00000697565.1:n.767C=
ENST00000697581.1:c.*821C=	ENSP00000513346.1:n.*821C=
ENST00000697582.1:c.827C=	ENSP00000513347.1:p.Thr276=
ENST00000697583.1:c.626C=	ENSP00000513349.1:p.Thr209=
ENST00000697584.1:c.626C=	ENSP00000513350.1:p.Thr209=
ENST00000697585.1:c.626C=	ENSP00000513351.1:p.Thr209=
ENST00000697586.1:c.626C=	ENSP00000513352.1:p.Thr209=
ENST00000697587.1:c.626C=	ENSP00000513353.1:p.Thr209=
ENST00000564138.6:c.827C= MANE Select	ENSP00000482457.1:p.Thr276=
ENST00000359376.7:c.827C=	ENSP00000352336.4:p.Thr276=
ENST00000563193.1:c.135C=
ENST00000564138.5:c.827C=	ENSP00000482457.1:p.Thr276=
ENST00000567980.5:n.1071C=
NM_002661.4:c.827C=	NP_002652.2:p.Thr276=
XM_011523108.1:c.941C=	XP_011521410.1:p.Thr314=
NM_002661.5:c.827C= MANE Select	NP_002652.2:p.Thr276=