Canonical Allele Identifier: CA8193359

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81880965C>G , CM000678.2:g.81880965C>G	GRCh38
NC_000016.9:g.81914570C>G , CM000678.1:g.81914570C>G	GRCh37
NC_000016.8:g.80472071C>G	NCBI36
NG_032019.2:g.146869C>G , LRG_376:g.146869C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.692+12C>G MANE Select	NP_002652.2:n.692+12C>G
ENST00000564138.6:c.692+12C>G MANE Select	ENSP00000482457.1:n.692+12C>G
NM_002661.4:c.692+12C>G	NP_002652.2:n.692+12C>G
ENST00000359376.7:c.692+12C>G	ENSP00000352336.4:n.692+12C>G
ENST00000563193.2:c.692+12C>G	ENSP00000455533.2:n.692+12C>G
ENST00000564138.5:c.692+12C>G	ENSP00000482457.1:n.692+12C>G
ENST00000567980.5:n.936+12C>G
ENST00000569929.5:n.728+12C>G
ENST00000697561.1:c.*121+12C>G	ENSP00000513337.1:n.*121+12C>G
ENST00000697562.1:c.692+12C>G	ENSP00000513338.1:n.692+12C>G
ENST00000697563.1:c.*265C>G	ENSP00000513339.1:n.*265C>G
ENST00000697564.1:c.649-8207C>G	ENSP00000513340.1:n.649-8207C>G
ENST00000697565.1:n.632+12C>G
ENST00000697581.1:c.*686+12C>G	ENSP00000513346.1:n.*686+12C>G
ENST00000697582.1:c.692+12C>G	ENSP00000513347.1:n.692+12C>G
ENST00000697583.1:c.491+12C>G	ENSP00000513349.1:n.491+12C>G
ENST00000697584.1:c.491+12C>G	ENSP00000513350.1:n.491+12C>G
ENST00000697585.1:c.491+12C>G	ENSP00000513351.1:n.491+12C>G
ENST00000697586.1:c.491+12C>G	ENSP00000513352.1:n.491+12C>G
ENST00000697587.1:c.491+12C>G	ENSP00000513353.1:n.491+12C>G
XM_011523108.1:c.806+12C>G	XP_011521410.1:n.806+12C>G