Canonical Allele Identifier: CA396897654

Gene: PLCG2

Linked Data

• MyVariant Identifiers: chr16:g.81922783T>G (hg19) ; chr16:g.81889178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889178T>G , CM000678.2:g.81889178T>G	GRCh38
NC_000016.9:g.81922783T>G , CM000678.1:g.81922783T>G	GRCh37
NC_000016.8:g.80480284T>G	NCBI36
NG_032019.2:g.155082T>G , LRG_376:g.155082T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.772T>G	ENSP00000455533.2:p.Trp258Gly
ENST00000697561.1:c.*201T>G	ENSP00000513337.1:n.*201T>G
ENST00000697562.1:c.772T>G	ENSP00000513338.1:p.Trp258Gly
ENST00000697563.1:c.*618T>G	ENSP00000513339.1:n.*618T>G
ENST00000697564.1:c.655T>G	ENSP00000513340.1:p.Trp219Gly
ENST00000697565.1:n.712T>G
ENST00000697581.1:c.*766T>G	ENSP00000513346.1:n.*766T>G
ENST00000697582.1:c.772T>G	ENSP00000513347.1:p.Trp258Gly
ENST00000697583.1:c.571T>G	ENSP00000513349.1:p.Trp191Gly
ENST00000697584.1:c.571T>G	ENSP00000513350.1:p.Trp191Gly
ENST00000697585.1:c.571T>G	ENSP00000513351.1:p.Trp191Gly
ENST00000697586.1:c.571T>G	ENSP00000513352.1:p.Trp191Gly
ENST00000697587.1:c.571T>G	ENSP00000513353.1:p.Trp191Gly
ENST00000564138.6:c.772T>G MANE Select	ENSP00000482457.1:p.Trp258Gly
ENST00000359376.7:c.772T>G	ENSP00000352336.4:p.Trp258Gly
ENST00000563193.1:c.80T>G
ENST00000564138.5:c.772T>G	ENSP00000482457.1:p.Trp258Gly
ENST00000567980.5:n.1016T>G
NM_002661.4:c.772T>G	NP_002652.2:p.Trp258Gly
XM_011523108.1:c.886T>G	XP_011521410.1:p.Trp296Gly
NM_002661.5:c.772T>G MANE Select	NP_002652.2:p.Trp258Gly