Canonical Allele Identifier: CA724736241

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81937909G>A , CM000678.2:g.81937909G>A	GRCh38
NC_000016.9:g.81971514G>A , CM000678.1:g.81971514G>A	GRCh37
NC_000016.8:g.80529015G>A	NCBI36
NG_032019.2:g.203813G>A , LRG_376:g.203813G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.3198+6G>A MANE Select	NP_002652.2:n.3198+6G>A
ENST00000564138.6:c.3198+6G>A MANE Select	ENSP00000482457.1:n.3198+6G>A
NM_002661.4:c.3198+6G>A	NP_002652.2:n.3198+6G>A
ENST00000359376.7:c.3198+6G>A	ENSP00000352336.4:n.3198+6G>A
ENST00000563269.2:n.1373+6G>A
ENST00000564138.5:c.3198+6G>A	ENSP00000482457.1:n.3198+6G>A
ENST00000567373.5:n.557+6G>A
ENST00000570198.2:n.2316+6G>A
ENST00000697562.1:c.*2058+6G>A	ENSP00000513338.1:n.*2058+6G>A
ENST00000697563.1:c.*3044+6G>A	ENSP00000513339.1:n.*3044+6G>A
ENST00000697564.1:c.3081+6G>A	ENSP00000513340.1:n.3081+6G>A
ENST00000697581.1:c.*3192+6G>A	ENSP00000513346.1:n.*3192+6G>A
ENST00000697582.1:c.*480+6G>A	ENSP00000513347.1:n.*480+6G>A
ENST00000697583.1:c.2997+6G>A	ENSP00000513349.1:n.2997+6G>A
ENST00000697584.1:c.2997+6G>A	ENSP00000513350.1:n.2997+6G>A
ENST00000697585.1:c.2997+6G>A	ENSP00000513351.1:n.2997+6G>A
ENST00000697586.1:c.2997+6G>A	ENSP00000513352.1:n.2997+6G>A
ENST00000697587.1:c.2997+6G>A	ENSP00000513353.1:n.2997+6G>A
XM_011523108.1:c.3312+6G>A	XP_011521410.1:n.3312+6G>A