Canonical Allele Identifier: CA2634519797

Gene: PLCG2

Linked Data

• gnomAD v4: 16-81889344-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889344T>C , CM000678.2:g.81889344T>C	GRCh38
NC_000016.9:g.81922949T>C , CM000678.1:g.81922949T>C	GRCh37
NC_000016.8:g.80480450T>C	NCBI36
NG_032019.2:g.155248T>C , LRG_376:g.155248T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+71T>C	ENSP00000455533.2:n.867+71T>C
ENST00000697561.1:c.*296+71T>C	ENSP00000513337.1:n.*296+71T>C
ENST00000697562.1:c.867+71T>C	ENSP00000513338.1:n.867+71T>C
ENST00000697563.1:c.*713+71T>C	ENSP00000513339.1:n.*713+71T>C
ENST00000697564.1:c.750+71T>C	ENSP00000513340.1:n.750+71T>C
ENST00000697565.1:n.807+71T>C
ENST00000697581.1:c.*861+71T>C	ENSP00000513346.1:n.*861+71T>C
ENST00000697582.1:c.867+71T>C	ENSP00000513347.1:n.867+71T>C
ENST00000697583.1:c.666+71T>C	ENSP00000513349.1:n.666+71T>C
ENST00000697584.1:c.666+71T>C	ENSP00000513350.1:n.666+71T>C
ENST00000697585.1:c.666+71T>C	ENSP00000513351.1:n.666+71T>C
ENST00000697586.1:c.666+71T>C	ENSP00000513352.1:n.666+71T>C
ENST00000697587.1:c.666+71T>C	ENSP00000513353.1:n.666+71T>C
ENST00000564138.6:c.867+71T>C MANE Select	ENSP00000482457.1:n.867+71T>C
ENST00000359376.7:c.867+71T>C	ENSP00000352336.4:n.867+71T>C
ENST00000562605.5:n.6T>C
ENST00000563193.1:c.175+71T>C
ENST00000564138.5:c.867+71T>C	ENSP00000482457.1:n.867+71T>C
ENST00000567980.5:n.1111+71T>C
NM_002661.4:c.867+71T>C	NP_002652.2:n.867+71T>C
XM_011523108.1:c.981+71T>C	XP_011521410.1:n.981+71T>C
NM_002661.5:c.867+71T>C MANE Select	NP_002652.2:n.867+71T>C