Canonical Allele Identifier: CA8193987

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81910724C>T , CM000678.2:g.81910724C>T	GRCh38
NC_000016.9:g.81944329C>T , CM000678.1:g.81944329C>T	GRCh37
NC_000016.8:g.80501830C>T	NCBI36
NG_032019.2:g.176628C>T , LRG_376:g.176628C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.1934+4C>T MANE Select	NP_002652.2:n.1934+4C>T
ENST00000564138.6:c.1934+4C>T MANE Select	ENSP00000482457.1:n.1934+4C>T
NM_002661.4:c.1934+4C>T	NP_002652.2:n.1934+4C>T
ENST00000359376.7:c.1934+4C>T	ENSP00000352336.4:n.1934+4C>T
ENST00000564138.5:c.1934+4C>T	ENSP00000482457.1:n.1934+4C>T
ENST00000567980.5:n.2178+4C>T
ENST00000570198.2:n.1052+4C>T
ENST00000697562.1:c.*794+4C>T	ENSP00000513338.1:n.*794+4C>T
ENST00000697563.1:c.*1780+4C>T	ENSP00000513339.1:n.*1780+4C>T
ENST00000697564.1:c.1817+4C>T	ENSP00000513340.1:n.1817+4C>T
ENST00000697581.1:c.*1928+4C>T	ENSP00000513346.1:n.*1928+4C>T
ENST00000697582.1:c.1934+4C>T	ENSP00000513347.1:n.1934+4C>T
ENST00000697583.1:c.1733+4C>T	ENSP00000513349.1:n.1733+4C>T
ENST00000697584.1:c.1733+4C>T	ENSP00000513350.1:n.1733+4C>T
ENST00000697585.1:c.1733+4C>T	ENSP00000513351.1:n.1733+4C>T
ENST00000697586.1:c.1733+4C>T	ENSP00000513352.1:n.1733+4C>T
ENST00000697587.1:c.1733+4C>T	ENSP00000513353.1:n.1733+4C>T
XM_011523108.1:c.2048+4C>T	XP_011521410.1:n.2048+4C>T