Canonical Allele Identifier: CA396900062

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81908423C>A , CM000678.2:g.81908423C>A	GRCh38
NC_000016.9:g.81942028C>A , CM000678.1:g.81942028C>A	GRCh37
NC_000016.8:g.80499529C>A	NCBI36
NG_032019.2:g.174327C>A , LRG_376:g.174327C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570198.2:n.683C>A
ENST00000697562.1:c.*425C>A	ENSP00000513338.1:n.*425C>A
ENST00000697563.1:c.*1411C>A	ENSP00000513339.1:n.*1411C>A
ENST00000697564.1:c.1448C>A	ENSP00000513340.1:p.Pro483His
ENST00000697581.1:c.*1559C>A	ENSP00000513346.1:n.*1559C>A
ENST00000697582.1:c.1565C>A	ENSP00000513347.1:p.Pro522His
ENST00000697583.1:c.1364C>A	ENSP00000513349.1:p.Pro455His
ENST00000697584.1:c.1364C>A	ENSP00000513350.1:p.Pro455His
ENST00000697585.1:c.1364C>A	ENSP00000513351.1:p.Pro455His
ENST00000697586.1:c.1364C>A	ENSP00000513352.1:p.Pro455His
ENST00000697587.1:c.1364C>A	ENSP00000513353.1:p.Pro455His
ENST00000564138.6:c.1565C>A MANE Select	ENSP00000482457.1:p.Pro522His
ENST00000359376.7:c.1565C>A	ENSP00000352336.4:p.Pro522His
ENST00000564138.5:c.1565C>A	ENSP00000482457.1:p.Pro522His
ENST00000567980.5:n.1809C>A
NM_002661.4:c.1565C>A	NP_002652.2:p.Pro522His
XM_011523108.1:c.1679C>A	XP_011521410.1:p.Pro560His
NM_002661.5:c.1565C>A MANE Select	NP_002652.2:p.Pro522His