Canonical Allele Identifier: CA396897757

Gene: PLCG2

Linked Data

• COSMIC: COSM4063144 ; COSM4063145
• MyVariant Identifiers: chr16:g.81922830T>G (hg19) ; chr16:g.81889225T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889225T>G , CM000678.2:g.81889225T>G	GRCh38
NC_000016.9:g.81922830T>G , CM000678.1:g.81922830T>G	GRCh37
NC_000016.8:g.80480331T>G	NCBI36
NG_032019.2:g.155129T>G , LRG_376:g.155129T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.819T>G	ENSP00000455533.2:p.Ile273Met
ENST00000697561.1:c.*248T>G	ENSP00000513337.1:n.*248T>G
ENST00000697562.1:c.819T>G	ENSP00000513338.1:p.Ile273Met
ENST00000697563.1:c.*665T>G	ENSP00000513339.1:n.*665T>G
ENST00000697564.1:c.702T>G	ENSP00000513340.1:p.Ile234Met
ENST00000697565.1:n.759T>G
ENST00000697581.1:c.*813T>G	ENSP00000513346.1:n.*813T>G
ENST00000697582.1:c.819T>G	ENSP00000513347.1:p.Ile273Met
ENST00000697583.1:c.618T>G	ENSP00000513349.1:p.Ile206Met
ENST00000697584.1:c.618T>G	ENSP00000513350.1:p.Ile206Met
ENST00000697585.1:c.618T>G	ENSP00000513351.1:p.Ile206Met
ENST00000697586.1:c.618T>G	ENSP00000513352.1:p.Ile206Met
ENST00000697587.1:c.618T>G	ENSP00000513353.1:p.Ile206Met
ENST00000564138.6:c.819T>G MANE Select	ENSP00000482457.1:p.Ile273Met
ENST00000359376.7:c.819T>G	ENSP00000352336.4:p.Ile273Met
ENST00000563193.1:c.127T>G
ENST00000564138.5:c.819T>G	ENSP00000482457.1:p.Ile273Met
ENST00000567980.5:n.1063T>G
NM_002661.4:c.819T>G	NP_002652.2:p.Ile273Met
XM_011523108.1:c.933T>G	XP_011521410.1:p.Ile311Met
NM_002661.5:c.819T>G MANE Select	NP_002652.2:p.Ile273Met