Canonical Allele Identifier: CA396897678

Gene: PLCG2

Linked Data

• MyVariant Identifiers: chr16:g.81922793A>C (hg19) ; chr16:g.81889188A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889188A>C , CM000678.2:g.81889188A>C	GRCh38
NC_000016.9:g.81922793A>C , CM000678.1:g.81922793A>C	GRCh37
NC_000016.8:g.80480294A>C	NCBI36
NG_032019.2:g.155092A>C , LRG_376:g.155092A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.782A>C	ENSP00000455533.2:p.Asp261Ala
ENST00000697561.1:c.*211A>C	ENSP00000513337.1:n.*211A>C
ENST00000697562.1:c.782A>C	ENSP00000513338.1:p.Asp261Ala
ENST00000697563.1:c.*628A>C	ENSP00000513339.1:n.*628A>C
ENST00000697564.1:c.665A>C	ENSP00000513340.1:p.Asp222Ala
ENST00000697565.1:n.722A>C
ENST00000697581.1:c.*776A>C	ENSP00000513346.1:n.*776A>C
ENST00000697582.1:c.782A>C	ENSP00000513347.1:p.Asp261Ala
ENST00000697583.1:c.581A>C	ENSP00000513349.1:p.Asp194Ala
ENST00000697584.1:c.581A>C	ENSP00000513350.1:p.Asp194Ala
ENST00000697585.1:c.581A>C	ENSP00000513351.1:p.Asp194Ala
ENST00000697586.1:c.581A>C	ENSP00000513352.1:p.Asp194Ala
ENST00000697587.1:c.581A>C	ENSP00000513353.1:p.Asp194Ala
ENST00000564138.6:c.782A>C MANE Select	ENSP00000482457.1:p.Asp261Ala
ENST00000359376.7:c.782A>C	ENSP00000352336.4:p.Asp261Ala
ENST00000563193.1:c.90A>C
ENST00000564138.5:c.782A>C	ENSP00000482457.1:p.Asp261Ala
ENST00000567980.5:n.1026A>C
NM_002661.4:c.782A>C	NP_002652.2:p.Asp261Ala
XM_011523108.1:c.896A>C	XP_011521410.1:p.Asp299Ala
NM_002661.5:c.782A>C MANE Select	NP_002652.2:p.Asp261Ala