Canonical Allele Identifier: CA396897652

Gene: PLCG2

Linked Data

• dbSNP Id: rs369555285
• MyVariant Identifiers: chr16:g.81922782T>G (hg19) ; chr16:g.81889177T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889177T>G , CM000678.2:g.81889177T>G	GRCh38
NC_000016.9:g.81922782T>G , CM000678.1:g.81922782T>G	GRCh37
NC_000016.8:g.80480283T>G	NCBI36
NG_032019.2:g.155081T>G , LRG_376:g.155081T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.771T>G	ENSP00000455533.2:p.His257Gln
ENST00000697561.1:c.*200T>G	ENSP00000513337.1:n.*200T>G
ENST00000697562.1:c.771T>G	ENSP00000513338.1:p.His257Gln
ENST00000697563.1:c.*617T>G	ENSP00000513339.1:n.*617T>G
ENST00000697564.1:c.654T>G	ENSP00000513340.1:p.His218Gln
ENST00000697565.1:n.711T>G
ENST00000697581.1:c.*765T>G	ENSP00000513346.1:n.*765T>G
ENST00000697582.1:c.771T>G	ENSP00000513347.1:p.His257Gln
ENST00000697583.1:c.570T>G	ENSP00000513349.1:p.His190Gln
ENST00000697584.1:c.570T>G	ENSP00000513350.1:p.His190Gln
ENST00000697585.1:c.570T>G	ENSP00000513351.1:p.His190Gln
ENST00000697586.1:c.570T>G	ENSP00000513352.1:p.His190Gln
ENST00000697587.1:c.570T>G	ENSP00000513353.1:p.His190Gln
ENST00000564138.6:c.771T>G MANE Select	ENSP00000482457.1:p.His257Gln
ENST00000359376.7:c.771T>G	ENSP00000352336.4:p.His257Gln
ENST00000563193.1:c.79T>G
ENST00000564138.5:c.771T>G	ENSP00000482457.1:p.His257Gln
ENST00000567980.5:n.1015T>G
NM_002661.4:c.771T>G	NP_002652.2:p.His257Gln
XM_011523108.1:c.885T>G	XP_011521410.1:p.His295Gln
NM_002661.5:c.771T>G MANE Select	NP_002652.2:p.His257Gln