Canonical Allele Identifier: CA623764572

Gene: PLCG2

Linked Data

• dbSNP Id: rs1451279988
• gnomAD v2: 16-81923158-T-A
• gnomAD v3: 16-81889553-T-A
• gnomAD v4: 16-81889553-T-A
• MyVariant Identifiers: chr16:g.81923158T>A (hg19) ; chr16:g.81889553T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889553T>A , CM000678.2:g.81889553T>A	GRCh38
NC_000016.9:g.81923158T>A , CM000678.1:g.81923158T>A	GRCh37
NC_000016.8:g.80480659T>A	NCBI36
NG_032019.2:g.155457T>A , LRG_376:g.155457T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+280T>A	ENSP00000455533.2:n.867+280T>A
ENST00000697561.1:c.*296+280T>A	ENSP00000513337.1:n.*296+280T>A
ENST00000697562.1:c.867+280T>A	ENSP00000513338.1:n.867+280T>A
ENST00000697563.1:c.*713+280T>A	ENSP00000513339.1:n.*713+280T>A
ENST00000697564.1:c.750+280T>A	ENSP00000513340.1:n.750+280T>A
ENST00000697565.1:n.807+280T>A
ENST00000697581.1:c.*861+280T>A	ENSP00000513346.1:n.*861+280T>A
ENST00000697582.1:c.867+280T>A	ENSP00000513347.1:n.867+280T>A
ENST00000697583.1:c.666+280T>A	ENSP00000513349.1:n.666+280T>A
ENST00000697584.1:c.666+280T>A	ENSP00000513350.1:n.666+280T>A
ENST00000697585.1:c.666+280T>A	ENSP00000513351.1:n.666+280T>A
ENST00000697586.1:c.666+280T>A	ENSP00000513352.1:n.666+280T>A
ENST00000697587.1:c.666+280T>A	ENSP00000513353.1:n.666+280T>A
ENST00000564138.6:c.867+280T>A MANE Select	ENSP00000482457.1:n.867+280T>A
ENST00000359376.7:c.867+280T>A	ENSP00000352336.4:n.867+280T>A
ENST00000562605.5:n.61+154T>A
ENST00000563193.1:c.175+280T>A
ENST00000564138.5:c.867+280T>A	ENSP00000482457.1:n.867+280T>A
ENST00000567980.5:n.1111+280T>A
NM_002661.4:c.867+280T>A	NP_002652.2:n.867+280T>A
XM_011523108.1:c.981+280T>A	XP_011521410.1:n.981+280T>A
NM_002661.5:c.867+280T>A MANE Select	NP_002652.2:n.867+280T>A