Canonical Allele Identifier: CA396897814

Gene: PLCG2

Linked Data

• MyVariant Identifiers: chr16:g.81922857G>C (hg19) ; chr16:g.81889252G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889252G>C , CM000678.2:g.81889252G>C	GRCh38
NC_000016.9:g.81922857G>C , CM000678.1:g.81922857G>C	GRCh37
NC_000016.8:g.80480358G>C	NCBI36
NG_032019.2:g.155156G>C , LRG_376:g.155156G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.846G>C	ENSP00000455533.2:p.Glu282Asp
ENST00000697561.1:c.*275G>C	ENSP00000513337.1:n.*275G>C
ENST00000697562.1:c.846G>C	ENSP00000513338.1:p.Glu282Asp
ENST00000697563.1:c.*692G>C	ENSP00000513339.1:n.*692G>C
ENST00000697564.1:c.729G>C	ENSP00000513340.1:p.Glu243Asp
ENST00000697565.1:n.786G>C
ENST00000697581.1:c.*840G>C	ENSP00000513346.1:n.*840G>C
ENST00000697582.1:c.846G>C	ENSP00000513347.1:p.Glu282Asp
ENST00000697583.1:c.645G>C	ENSP00000513349.1:p.Glu215Asp
ENST00000697584.1:c.645G>C	ENSP00000513350.1:p.Glu215Asp
ENST00000697585.1:c.645G>C	ENSP00000513351.1:p.Glu215Asp
ENST00000697586.1:c.645G>C	ENSP00000513352.1:p.Glu215Asp
ENST00000697587.1:c.645G>C	ENSP00000513353.1:p.Glu215Asp
ENST00000564138.6:c.846G>C MANE Select	ENSP00000482457.1:p.Glu282Asp
ENST00000359376.7:c.846G>C	ENSP00000352336.4:p.Glu282Asp
ENST00000563193.1:c.154G>C
ENST00000564138.5:c.846G>C	ENSP00000482457.1:p.Glu282Asp
ENST00000567980.5:n.1090G>C
NM_002661.4:c.846G>C	NP_002652.2:p.Glu282Asp
XM_011523108.1:c.960G>C	XP_011521410.1:p.Glu320Asp
NM_002661.5:c.846G>C MANE Select	NP_002652.2:p.Glu282Asp