Canonical Allele Identifier: CA623764571

Gene: PLCG2

Linked Data

• dbSNP Id: rs1344389488
• gnomAD v2: 16-81923155-A-T
• gnomAD v3: 16-81889550-A-T
• gnomAD v4: 16-81889550-A-T
• MyVariant Identifiers: chr16:g.81923155A>T (hg19) ; chr16:g.81889550A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889550A>T , CM000678.2:g.81889550A>T	GRCh38
NC_000016.9:g.81923155A>T , CM000678.1:g.81923155A>T	GRCh37
NC_000016.8:g.80480656A>T	NCBI36
NG_032019.2:g.155454A>T , LRG_376:g.155454A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+277A>T	ENSP00000455533.2:n.867+277A>T
ENST00000697561.1:c.*296+277A>T	ENSP00000513337.1:n.*296+277A>T
ENST00000697562.1:c.867+277A>T	ENSP00000513338.1:n.867+277A>T
ENST00000697563.1:c.*713+277A>T	ENSP00000513339.1:n.*713+277A>T
ENST00000697564.1:c.750+277A>T	ENSP00000513340.1:n.750+277A>T
ENST00000697565.1:n.807+277A>T
ENST00000697581.1:c.*861+277A>T	ENSP00000513346.1:n.*861+277A>T
ENST00000697582.1:c.867+277A>T	ENSP00000513347.1:n.867+277A>T
ENST00000697583.1:c.666+277A>T	ENSP00000513349.1:n.666+277A>T
ENST00000697584.1:c.666+277A>T	ENSP00000513350.1:n.666+277A>T
ENST00000697585.1:c.666+277A>T	ENSP00000513351.1:n.666+277A>T
ENST00000697586.1:c.666+277A>T	ENSP00000513352.1:n.666+277A>T
ENST00000697587.1:c.666+277A>T	ENSP00000513353.1:n.666+277A>T
ENST00000564138.6:c.867+277A>T MANE Select	ENSP00000482457.1:n.867+277A>T
ENST00000359376.7:c.867+277A>T	ENSP00000352336.4:n.867+277A>T
ENST00000562605.5:n.61+151A>T
ENST00000563193.1:c.175+277A>T
ENST00000564138.5:c.867+277A>T	ENSP00000482457.1:n.867+277A>T
ENST00000567980.5:n.1111+277A>T
NM_002661.4:c.867+277A>T	NP_002652.2:n.867+277A>T
XM_011523108.1:c.981+277A>T	XP_011521410.1:n.981+277A>T
NM_002661.5:c.867+277A>T MANE Select	NP_002652.2:n.867+277A>T