Canonical Allele Identifier: CA396897820

Gene: PLCG2

Linked Data

• gnomAD v4: 16-81889254-C-A
• MyVariant Identifiers: chr16:g.81922859C>A (hg19) ; chr16:g.81889254C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889254C>A , CM000678.2:g.81889254C>A	GRCh38
NC_000016.9:g.81922859C>A , CM000678.1:g.81922859C>A	GRCh37
NC_000016.8:g.80480360C>A	NCBI36
NG_032019.2:g.155158C>A , LRG_376:g.155158C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.848C>A	ENSP00000455533.2:p.Pro283His
ENST00000697561.1:c.*277C>A	ENSP00000513337.1:n.*277C>A
ENST00000697562.1:c.848C>A	ENSP00000513338.1:p.Pro283His
ENST00000697563.1:c.*694C>A	ENSP00000513339.1:n.*694C>A
ENST00000697564.1:c.731C>A	ENSP00000513340.1:p.Pro244His
ENST00000697565.1:n.788C>A
ENST00000697581.1:c.*842C>A	ENSP00000513346.1:n.*842C>A
ENST00000697582.1:c.848C>A	ENSP00000513347.1:p.Pro283His
ENST00000697583.1:c.647C>A	ENSP00000513349.1:p.Pro216His
ENST00000697584.1:c.647C>A	ENSP00000513350.1:p.Pro216His
ENST00000697585.1:c.647C>A	ENSP00000513351.1:p.Pro216His
ENST00000697586.1:c.647C>A	ENSP00000513352.1:p.Pro216His
ENST00000697587.1:c.647C>A	ENSP00000513353.1:p.Pro216His
ENST00000564138.6:c.848C>A MANE Select	ENSP00000482457.1:p.Pro283His
ENST00000359376.7:c.848C>A	ENSP00000352336.4:p.Pro283His
ENST00000563193.1:c.156C>A
ENST00000564138.5:c.848C>A	ENSP00000482457.1:p.Pro283His
ENST00000567980.5:n.1092C>A
NM_002661.4:c.848C>A	NP_002652.2:p.Pro283His
XM_011523108.1:c.962C>A	XP_011521410.1:p.Pro321His
NM_002661.5:c.848C>A MANE Select	NP_002652.2:p.Pro283His