Canonical Allele Identifier: CA979668751

Gene: PLCG2

Linked Data

• dbSNP Id: rs1908508524
• gnomAD v3: 16-81889079-T-TC
• gnomAD v4: 16-81889079-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889080dup , CM000678.2:g.81889080dup	GRCh38
NC_000016.9:g.81922685dup , CM000678.1:g.81922685dup	GRCh37
NC_000016.8:g.80480186dup	NCBI36
NG_032019.2:g.154984dup , LRG_376:g.154984dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.766-92dup	ENSP00000455533.2:n.766-92dup
ENST00000697561.1:c.*195-92dup	ENSP00000513337.1:n.*195-92dup
ENST00000697562.1:c.766-92dup	ENSP00000513338.1:n.766-92dup
ENST00000697563.1:c.*612-92dup	ENSP00000513339.1:n.*612-92dup
ENST00000697564.1:c.649-92dup	ENSP00000513340.1:n.649-92dup
ENST00000697565.1:n.706-92dup
ENST00000697581.1:c.*760-92dup	ENSP00000513346.1:n.*760-92dup
ENST00000697582.1:c.766-92dup	ENSP00000513347.1:n.766-92dup
ENST00000697583.1:c.565-92dup	ENSP00000513349.1:n.565-92dup
ENST00000697584.1:c.565-92dup	ENSP00000513350.1:n.565-92dup
ENST00000697585.1:c.565-92dup	ENSP00000513351.1:n.565-92dup
ENST00000697586.1:c.565-92dup	ENSP00000513352.1:n.565-92dup
ENST00000697587.1:c.565-92dup	ENSP00000513353.1:n.565-92dup
ENST00000564138.6:c.766-92dup MANE Select	ENSP00000482457.1:n.766-92dup
ENST00000359376.7:c.766-92dup	ENSP00000352336.4:n.766-92dup
ENST00000563193.1:c.74-92dup
ENST00000564138.5:c.766-92dup	ENSP00000482457.1:n.766-92dup
ENST00000567980.5:n.1010-92dup
NM_002661.4:c.766-92dup	NP_002652.2:n.766-92dup
XM_011523108.1:c.880-92dup	XP_011521410.1:n.880-92dup
NM_002661.5:c.766-92dup MANE Select	NP_002652.2:n.766-92dup