Canonical Allele Identifier: CA8194036

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81912673A>G , CM000678.2:g.81912673A>G	GRCh38
NC_000016.9:g.81946278A>G , CM000678.1:g.81946278A>G	GRCh37
NC_000016.8:g.80503779A>G	NCBI36
NG_032019.2:g.178577A>G , LRG_376:g.178577A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570198.2:n.1129A>G
ENST00000697562.1:c.*871A>G	ENSP00000513338.1:n.*871A>G
ENST00000697563.1:c.*1857A>G	ENSP00000513339.1:n.*1857A>G
ENST00000697564.1:c.1894A>G	ENSP00000513340.1:p.Ile632Val
ENST00000697581.1:c.*2005A>G	ENSP00000513346.1:n.*2005A>G
ENST00000697582.1:c.2011A>G	ENSP00000513347.1:p.Ile671Val
ENST00000697583.1:c.1810A>G	ENSP00000513349.1:p.Ile604Val
ENST00000697584.1:c.1810A>G	ENSP00000513350.1:p.Ile604Val
ENST00000697585.1:c.1810A>G	ENSP00000513351.1:p.Ile604Val
ENST00000697586.1:c.1810A>G	ENSP00000513352.1:p.Ile604Val
ENST00000697587.1:c.1810A>G	ENSP00000513353.1:p.Ile604Val
ENST00000564138.6:c.2011A>G MANE Select	ENSP00000482457.1:p.Ile671Val
ENST00000359376.7:c.2011A>G	ENSP00000352336.4:p.Ile671Val
ENST00000564138.5:c.2011A>G	ENSP00000482457.1:p.Ile671Val
ENST00000567980.5:n.2255A>G
NM_002661.4:c.2011A>G	NP_002652.2:p.Ile671Val
XM_011523108.1:c.2125A>G	XP_011521410.1:p.Ile709Val
NM_002661.5:c.2011A>G MANE Select	NP_002652.2:p.Ile671Val