Canonical Allele Identifier: CA8194351

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81928634C>G , CM000678.2:g.81928634C>G	GRCh38
NC_000016.9:g.81962239C>G , CM000678.1:g.81962239C>G	GRCh37
NC_000016.8:g.80519740C>G	NCBI36
NG_032019.2:g.194538C>G , LRG_376:g.194538C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.2581+10C>G MANE Select	NP_002652.2:n.2581+10C>G
ENST00000564138.6:c.2581+10C>G MANE Select	ENSP00000482457.1:n.2581+10C>G
NM_002661.4:c.2581+10C>G	NP_002652.2:n.2581+10C>G
ENST00000359376.7:c.2581+10C>G	ENSP00000352336.4:n.2581+10C>G
ENST00000564138.5:c.2581+10C>G	ENSP00000482457.1:n.2581+10C>G
ENST00000570196.1:n.354C>G
ENST00000570198.2:n.1699+10C>G
ENST00000697562.1:c.*1441+10C>G	ENSP00000513338.1:n.*1441+10C>G
ENST00000697563.1:c.*2427+10C>G	ENSP00000513339.1:n.*2427+10C>G
ENST00000697564.1:c.2464+10C>G	ENSP00000513340.1:n.2464+10C>G
ENST00000697581.1:c.*2575+10C>G	ENSP00000513346.1:n.*2575+10C>G
ENST00000697582.1:c.2581+10C>G	ENSP00000513347.1:n.2581+10C>G
ENST00000697583.1:c.2380+10C>G	ENSP00000513349.1:n.2380+10C>G
ENST00000697584.1:c.2380+10C>G	ENSP00000513350.1:n.2380+10C>G
ENST00000697585.1:c.2380+10C>G	ENSP00000513351.1:n.2380+10C>G
ENST00000697586.1:c.2380+10C>G	ENSP00000513352.1:n.2380+10C>G
ENST00000697587.1:c.2380+10C>G	ENSP00000513353.1:n.2380+10C>G
XM_011523108.1:c.2695+10C>G	XP_011521410.1:n.2695+10C>G