Canonical Allele Identifier: CA8193467

Gene: PLCG2

Linked Data

• dbSNP Id: rs749902171
• ExAC: 16:81922853 C / A
• gnomAD v2: 16-81922853-C-A
• gnomAD v4: 16-81889248-C-A
• MyVariant Identifiers: chr16:g.81922853C>A (hg19) ; chr16:g.81889248C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889248C>A , CM000678.2:g.81889248C>A	GRCh38
NC_000016.9:g.81922853C>A , CM000678.1:g.81922853C>A	GRCh37
NC_000016.8:g.80480354C>A	NCBI36
NG_032019.2:g.155152C>A , LRG_376:g.155152C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.842C>A	ENSP00000455533.2:p.Ala281Asp
ENST00000697561.1:c.*271C>A	ENSP00000513337.1:n.*271C>A
ENST00000697562.1:c.842C>A	ENSP00000513338.1:p.Ala281Asp
ENST00000697563.1:c.*688C>A	ENSP00000513339.1:n.*688C>A
ENST00000697564.1:c.725C>A	ENSP00000513340.1:p.Ala242Asp
ENST00000697565.1:n.782C>A
ENST00000697581.1:c.*836C>A	ENSP00000513346.1:n.*836C>A
ENST00000697582.1:c.842C>A	ENSP00000513347.1:p.Ala281Asp
ENST00000697583.1:c.641C>A	ENSP00000513349.1:p.Ala214Asp
ENST00000697584.1:c.641C>A	ENSP00000513350.1:p.Ala214Asp
ENST00000697585.1:c.641C>A	ENSP00000513351.1:p.Ala214Asp
ENST00000697586.1:c.641C>A	ENSP00000513352.1:p.Ala214Asp
ENST00000697587.1:c.641C>A	ENSP00000513353.1:p.Ala214Asp
ENST00000564138.6:c.842C>A MANE Select	ENSP00000482457.1:p.Ala281Asp
ENST00000359376.7:c.842C>A	ENSP00000352336.4:p.Ala281Asp
ENST00000563193.1:c.150C>A
ENST00000564138.5:c.842C>A	ENSP00000482457.1:p.Ala281Asp
ENST00000567980.5:n.1086C>A
NM_002661.4:c.842C>A	NP_002652.2:p.Ala281Asp
XM_011523108.1:c.956C>A	XP_011521410.1:p.Ala319Asp
NM_002661.5:c.842C>A MANE Select	NP_002652.2:p.Ala281Asp