Canonical Allele Identifier: CA396897675

Gene: PLCG2

Linked Data

• gnomAD v4: 16-81889187-G-A
• MyVariant Identifiers: chr16:g.81922792G>A (hg19) ; chr16:g.81889187G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889187G>A , CM000678.2:g.81889187G>A	GRCh38
NC_000016.9:g.81922792G>A , CM000678.1:g.81922792G>A	GRCh37
NC_000016.8:g.80480293G>A	NCBI36
NG_032019.2:g.155091G>A , LRG_376:g.155091G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.781G>A	ENSP00000455533.2:p.Asp261Asn
ENST00000697561.1:c.*210G>A	ENSP00000513337.1:n.*210G>A
ENST00000697562.1:c.781G>A	ENSP00000513338.1:p.Asp261Asn
ENST00000697563.1:c.*627G>A	ENSP00000513339.1:n.*627G>A
ENST00000697564.1:c.664G>A	ENSP00000513340.1:p.Asp222Asn
ENST00000697565.1:n.721G>A
ENST00000697581.1:c.*775G>A	ENSP00000513346.1:n.*775G>A
ENST00000697582.1:c.781G>A	ENSP00000513347.1:p.Asp261Asn
ENST00000697583.1:c.580G>A	ENSP00000513349.1:p.Asp194Asn
ENST00000697584.1:c.580G>A	ENSP00000513350.1:p.Asp194Asn
ENST00000697585.1:c.580G>A	ENSP00000513351.1:p.Asp194Asn
ENST00000697586.1:c.580G>A	ENSP00000513352.1:p.Asp194Asn
ENST00000697587.1:c.580G>A	ENSP00000513353.1:p.Asp194Asn
ENST00000564138.6:c.781G>A MANE Select	ENSP00000482457.1:p.Asp261Asn
ENST00000359376.7:c.781G>A	ENSP00000352336.4:p.Asp261Asn
ENST00000563193.1:c.89G>A
ENST00000564138.5:c.781G>A	ENSP00000482457.1:p.Asp261Asn
ENST00000567980.5:n.1025G>A
NM_002661.4:c.781G>A	NP_002652.2:p.Asp261Asn
XM_011523108.1:c.895G>A	XP_011521410.1:p.Asp299Asn
NM_002661.5:c.781G>A MANE Select	NP_002652.2:p.Asp261Asn