Canonical Allele Identifier: CA496699185

Gene: PLCG2

Linked Data

• MyVariant Identifiers: chr16:g.81922788T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889183T>C , CM000678.2:g.81889183T>C	GRCh38
NC_000016.9:g.81922788T>C , CM000678.1:g.81922788T>C	GRCh37
NC_000016.8:g.80480289T>C	NCBI36
NG_032019.2:g.155087T>C , LRG_376:g.155087T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.777T>C	ENSP00000455533.2:p.Ala259=
ENST00000697561.1:c.*206T>C	ENSP00000513337.1:n.*206T>C
ENST00000697562.1:c.777T>C	ENSP00000513338.1:p.Ala259=
ENST00000697563.1:c.*623T>C	ENSP00000513339.1:n.*623T>C
ENST00000697564.1:c.660T>C	ENSP00000513340.1:p.Ala220=
ENST00000697565.1:n.717T>C
ENST00000697581.1:c.*771T>C	ENSP00000513346.1:n.*771T>C
ENST00000697582.1:c.777T>C	ENSP00000513347.1:p.Ala259=
ENST00000697583.1:c.576T>C	ENSP00000513349.1:p.Ala192=
ENST00000697584.1:c.576T>C	ENSP00000513350.1:p.Ala192=
ENST00000697585.1:c.576T>C	ENSP00000513351.1:p.Ala192=
ENST00000697586.1:c.576T>C	ENSP00000513352.1:p.Ala192=
ENST00000697587.1:c.576T>C	ENSP00000513353.1:p.Ala192=
ENST00000564138.6:c.777T>C MANE Select	ENSP00000482457.1:p.Ala259=
ENST00000359376.7:c.777T>C	ENSP00000352336.4:p.Ala259=
ENST00000563193.1:c.85T>C
ENST00000564138.5:c.777T>C	ENSP00000482457.1:p.Ala259=
ENST00000567980.5:n.1021T>C
NM_002661.4:c.777T>C	NP_002652.2:p.Ala259=
XM_011523108.1:c.891T>C	XP_011521410.1:p.Ala297=
NM_002661.5:c.777T>C MANE Select	NP_002652.2:p.Ala259=