Canonical Allele Identifier: CA8193630

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81895922C>G , CM000678.2:g.81895922C>G	GRCh38
NC_000016.9:g.81929527C>G , CM000678.1:g.81929527C>G	GRCh37
NC_000016.8:g.80487028C>G	NCBI36
NG_032019.2:g.161826C>G , LRG_376:g.161826C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.1188C>G	ENSP00000455533.2:p.Thr396=
ENST00000563375.2:c.176C>G
ENST00000570198.2:n.306C>G
ENST00000697562.1:c.1188C>G	ENSP00000513338.1:p.Thr396=
ENST00000697563.1:c.*1034C>G	ENSP00000513339.1:n.*1034C>G
ENST00000697564.1:c.1071C>G	ENSP00000513340.1:p.Thr357=
ENST00000697565.1:n.1128C>G
ENST00000697581.1:c.*1182C>G	ENSP00000513346.1:n.*1182C>G
ENST00000697582.1:c.1188C>G	ENSP00000513347.1:p.Thr396=
ENST00000697583.1:c.987C>G	ENSP00000513349.1:p.Thr329=
ENST00000697584.1:c.987C>G	ENSP00000513350.1:p.Thr329=
ENST00000697585.1:c.987C>G	ENSP00000513351.1:p.Thr329=
ENST00000697586.1:c.987C>G	ENSP00000513352.1:p.Thr329=
ENST00000697587.1:c.987C>G	ENSP00000513353.1:p.Thr329=
ENST00000564138.6:c.1188C>G MANE Select	ENSP00000482457.1:p.Thr396=
ENST00000359376.7:c.1188C>G	ENSP00000352336.4:p.Thr396=
ENST00000562605.5:n.382C>G
ENST00000563193.1:c.496C>G
ENST00000563375.1:c.176C>G
ENST00000564138.5:c.1188C>G	ENSP00000482457.1:p.Thr396=
ENST00000567980.5:n.1432C>G
ENST00000570198.1:n.304C>G
NM_002661.4:c.1188C>G	NP_002652.2:p.Thr396=
XM_011523108.1:c.1302C>G	XP_011521410.1:p.Thr434=
NM_002661.5:c.1188C>G MANE Select	NP_002652.2:p.Thr396=