Canonical Allele Identifier: CA285204810

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81956781A>T , CM000678.2:g.81956781A>T	GRCh38
NC_000016.9:g.81990386A>T , CM000678.1:g.81990386A>T	GRCh37
NC_000016.8:g.80547887A>T	NCBI36
NG_032019.2:g.222685A>T , LRG_376:g.222685A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563269.2:n.1832A>T
ENST00000570198.2:n.2775A>T
ENST00000697562.1:c.*2517A>T	ENSP00000513338.1:n.*2517A>T
ENST00000697563.1:c.*3503A>T	ENSP00000513339.1:n.*3503A>T
ENST00000697564.1:c.3540A>T	ENSP00000513340.1:p.Thr1180=
ENST00000697581.1:c.*3651A>T	ENSP00000513346.1:n.*3651A>T
ENST00000697582.1:c.*939A>T	ENSP00000513347.1:n.*939A>T
ENST00000697583.1:c.3456A>T	ENSP00000513349.1:p.Thr1152=
ENST00000697584.1:c.3456A>T	ENSP00000513350.1:p.Thr1152=
ENST00000697585.1:c.3456A>T	ENSP00000513351.1:p.Thr1152=
ENST00000697586.1:c.3456A>T	ENSP00000513352.1:p.Thr1152=
ENST00000697587.1:c.3456A>T	ENSP00000513353.1:p.Thr1152=
ENST00000564138.6:c.3657A>T MANE Select	ENSP00000482457.1:p.Thr1219=
ENST00000359376.7:c.3657A>T	ENSP00000352336.4:p.Thr1219=
ENST00000564138.5:c.3657A>T	ENSP00000482457.1:p.Thr1219=
NM_002661.4:c.3657A>T	NP_002652.2:p.Thr1219=
XM_011523108.1:c.3771A>T	XP_011521410.1:p.Thr1257=
NM_002661.5:c.3657A>T MANE Select	NP_002652.2:p.Thr1219=