Canonical Allele Identifier: CA8194747

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81946172C>T , CM000678.2:g.81946172C>T	GRCh38
NC_000016.9:g.81979777C>T , CM000678.1:g.81979777C>T	GRCh37
NC_000016.8:g.80537278C>T	NCBI36
NG_032019.2:g.212076C>T , LRG_376:g.212076C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563269.2:n.1657-3C>T
ENST00000570198.2:n.2600-3C>T
ENST00000697562.1:c.*2342-3C>T	ENSP00000513338.1:n.*2342-3C>T
ENST00000697563.1:c.*3328-3C>T	ENSP00000513339.1:n.*3328-3C>T
ENST00000697564.1:c.3365-3C>T	ENSP00000513340.1:n.3365-3C>T
ENST00000697581.1:c.*3476-3C>T	ENSP00000513346.1:n.*3476-3C>T
ENST00000697582.1:c.*764-3C>T	ENSP00000513347.1:n.*764-3C>T
ENST00000697583.1:c.3281-3C>T	ENSP00000513349.1:n.3281-3C>T
ENST00000697584.1:c.3281-3C>T	ENSP00000513350.1:n.3281-3C>T
ENST00000697585.1:c.3281-3C>T	ENSP00000513351.1:n.3281-3C>T
ENST00000697586.1:c.3281-3C>T	ENSP00000513352.1:n.3281-3C>T
ENST00000697587.1:c.3281-3C>T	ENSP00000513353.1:n.3281-3C>T
ENST00000564138.6:c.3482-3C>T MANE Select	ENSP00000482457.1:n.3482-3C>T
ENST00000359376.7:c.3482-3C>T	ENSP00000352336.4:n.3482-3C>T
ENST00000564138.5:c.3482-3C>T	ENSP00000482457.1:n.3482-3C>T
ENST00000567356.1:n.457-3C>T
NM_002661.4:c.3482-3C>T	NP_002652.2:n.3482-3C>T
XM_011523108.1:c.3596-3C>T	XP_011521410.1:n.3596-3C>T
NM_002661.5:c.3482-3C>T MANE Select	NP_002652.2:n.3482-3C>T