Canonical Allele Identifier: CA8193405

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81883307A>G , CM000678.2:g.81883307A>G	GRCh38
NC_000016.9:g.81916912A>G , CM000678.1:g.81916912A>G	GRCh37
NC_000016.8:g.80474413A>G	NCBI36
NG_032019.2:g.149211A>G , LRG_376:g.149211A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.731A>G	ENSP00000455533.2:p.His244Arg
ENST00000697561.1:c.*160A>G	ENSP00000513337.1:n.*160A>G
ENST00000697562.1:c.731A>G	ENSP00000513338.1:p.His244Arg
ENST00000697563.1:c.*577A>G	ENSP00000513339.1:n.*577A>G
ENST00000697564.1:c.649-5865A>G	ENSP00000513340.1:n.649-5865A>G
ENST00000697565.1:n.671A>G
ENST00000697581.1:c.*725A>G	ENSP00000513346.1:n.*725A>G
ENST00000697582.1:c.731A>G	ENSP00000513347.1:p.His244Arg
ENST00000697583.1:c.530A>G	ENSP00000513349.1:p.His177Arg
ENST00000697584.1:c.530A>G	ENSP00000513350.1:p.His177Arg
ENST00000697585.1:c.530A>G	ENSP00000513351.1:p.His177Arg
ENST00000697586.1:c.530A>G	ENSP00000513352.1:p.His177Arg
ENST00000697587.1:c.530A>G	ENSP00000513353.1:p.His177Arg
ENST00000564138.6:c.731A>G MANE Select	ENSP00000482457.1:p.His244Arg
ENST00000359376.7:c.731A>G	ENSP00000352336.4:p.His244Arg
ENST00000563193.1:c.39A>G
ENST00000564138.5:c.731A>G	ENSP00000482457.1:p.His244Arg
ENST00000567980.5:n.975A>G
ENST00000569929.5:n.767A>G
NM_002661.4:c.731A>G	NP_002652.2:p.His244Arg
XM_011523108.1:c.845A>G	XP_011521410.1:p.His282Arg
NM_002661.5:c.731A>G MANE Select	NP_002652.2:p.His244Arg