Canonical Allele Identifier: CA8193269

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81869317C>T , CM000678.2:g.81869317C>T	GRCh38
NC_000016.9:g.81902922C>T , CM000678.1:g.81902922C>T	GRCh37
NC_000016.8:g.80460423C>T	NCBI36
NG_032019.2:g.135221C>T , LRG_376:g.135221C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.564+19C>T MANE Select	NP_002652.2:n.564+19C>T
ENST00000564138.6:c.564+19C>T MANE Select	ENSP00000482457.1:n.564+19C>T
NM_002661.4:c.564+19C>T	NP_002652.2:n.564+19C>T
ENST00000359376.7:c.564+19C>T	ENSP00000352336.4:n.564+19C>T
ENST00000563193.2:c.564+19C>T	ENSP00000455533.2:n.564+19C>T
ENST00000564138.5:c.564+19C>T	ENSP00000482457.1:n.564+19C>T
ENST00000567980.5:n.808+19C>T
ENST00000569929.5:n.600+19C>T
ENST00000697561.1:c.564+19C>T	ENSP00000513337.1:n.564+19C>T
ENST00000697562.1:c.564+19C>T	ENSP00000513338.1:n.564+19C>T
ENST00000697563.1:c.*125+19C>T	ENSP00000513339.1:n.*125+19C>T
ENST00000697564.1:c.564+19C>T	ENSP00000513340.1:n.564+19C>T
ENST00000697565.1:n.504+19C>T
ENST00000697581.1:c.*558+19C>T	ENSP00000513346.1:n.*558+19C>T
ENST00000697582.1:c.564+19C>T	ENSP00000513347.1:n.564+19C>T
ENST00000697583.1:c.363+19C>T	ENSP00000513349.1:n.363+19C>T
ENST00000697584.1:c.363+19C>T	ENSP00000513350.1:n.363+19C>T
ENST00000697585.1:c.363+19C>T	ENSP00000513351.1:n.363+19C>T
ENST00000697586.1:c.363+19C>T	ENSP00000513352.1:n.363+19C>T
ENST00000697587.1:c.363+19C>T	ENSP00000513353.1:n.363+19C>T
XM_011523108.1:c.678+19C>T	XP_011521410.1:n.678+19C>T