Canonical Allele Identifier: CA396897692

Gene: PLCG2

Linked Data

• MyVariant Identifiers: chr16:g.81922799A>T (hg19) ; chr16:g.81889194A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889194A>T , CM000678.2:g.81889194A>T	GRCh38
NC_000016.9:g.81922799A>T , CM000678.1:g.81922799A>T	GRCh37
NC_000016.8:g.80480300A>T	NCBI36
NG_032019.2:g.155098A>T , LRG_376:g.155098A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.788A>T	ENSP00000455533.2:p.Asn263Ile
ENST00000697561.1:c.*217A>T	ENSP00000513337.1:n.*217A>T
ENST00000697562.1:c.788A>T	ENSP00000513338.1:p.Asn263Ile
ENST00000697563.1:c.*634A>T	ENSP00000513339.1:n.*634A>T
ENST00000697564.1:c.671A>T	ENSP00000513340.1:p.Asn224Ile
ENST00000697565.1:n.728A>T
ENST00000697581.1:c.*782A>T	ENSP00000513346.1:n.*782A>T
ENST00000697582.1:c.788A>T	ENSP00000513347.1:p.Asn263Ile
ENST00000697583.1:c.587A>T	ENSP00000513349.1:p.Asn196Ile
ENST00000697584.1:c.587A>T	ENSP00000513350.1:p.Asn196Ile
ENST00000697585.1:c.587A>T	ENSP00000513351.1:p.Asn196Ile
ENST00000697586.1:c.587A>T	ENSP00000513352.1:p.Asn196Ile
ENST00000697587.1:c.587A>T	ENSP00000513353.1:p.Asn196Ile
ENST00000564138.6:c.788A>T MANE Select	ENSP00000482457.1:p.Asn263Ile
ENST00000359376.7:c.788A>T	ENSP00000352336.4:p.Asn263Ile
ENST00000563193.1:c.96A>T
ENST00000564138.5:c.788A>T	ENSP00000482457.1:p.Asn263Ile
ENST00000567980.5:n.1032A>T
NM_002661.4:c.788A>T	NP_002652.2:p.Asn263Ile
XM_011523108.1:c.902A>T	XP_011521410.1:p.Asn301Ile
NM_002661.5:c.788A>T MANE Select	NP_002652.2:p.Asn263Ile