Canonical Allele Identifier: CA2634519749

Gene: PLCG2

Linked Data

• gnomAD v4: 16-81889276-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889276G>T , CM000678.2:g.81889276G>T	GRCh38
NC_000016.9:g.81922881G>T , CM000678.1:g.81922881G>T	GRCh37
NC_000016.8:g.80480382G>T	NCBI36
NG_032019.2:g.155180G>T , LRG_376:g.155180G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+3G>T	ENSP00000455533.2:n.867+3G>T
ENST00000697561.1:c.*296+3G>T	ENSP00000513337.1:n.*296+3G>T
ENST00000697562.1:c.867+3G>T	ENSP00000513338.1:n.867+3G>T
ENST00000697563.1:c.*713+3G>T	ENSP00000513339.1:n.*713+3G>T
ENST00000697564.1:c.750+3G>T	ENSP00000513340.1:n.750+3G>T
ENST00000697565.1:n.807+3G>T
ENST00000697581.1:c.*861+3G>T	ENSP00000513346.1:n.*861+3G>T
ENST00000697582.1:c.867+3G>T	ENSP00000513347.1:n.867+3G>T
ENST00000697583.1:c.666+3G>T	ENSP00000513349.1:n.666+3G>T
ENST00000697584.1:c.666+3G>T	ENSP00000513350.1:n.666+3G>T
ENST00000697585.1:c.666+3G>T	ENSP00000513351.1:n.666+3G>T
ENST00000697586.1:c.666+3G>T	ENSP00000513352.1:n.666+3G>T
ENST00000697587.1:c.666+3G>T	ENSP00000513353.1:n.666+3G>T
ENST00000564138.6:c.867+3G>T MANE Select	ENSP00000482457.1:n.867+3G>T
ENST00000359376.7:c.867+3G>T	ENSP00000352336.4:n.867+3G>T
ENST00000563193.1:c.175+3G>T
ENST00000564138.5:c.867+3G>T	ENSP00000482457.1:n.867+3G>T
ENST00000567980.5:n.1111+3G>T
NM_002661.4:c.867+3G>T	NP_002652.2:n.867+3G>T
XM_011523108.1:c.981+3G>T	XP_011521410.1:n.981+3G>T
NM_002661.5:c.867+3G>T MANE Select	NP_002652.2:n.867+3G>T