Canonical Allele Identifier: CA8193017

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81786066C>T , CM000678.2:g.81786066C>T	GRCh38
NC_000016.9:g.81819671C>T , CM000678.1:g.81819671C>T	GRCh37
NC_000016.8:g.80377172C>T	NCBI36
NG_032019.2:g.51970C>T , LRG_376:g.51970C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.77C>T MANE Select	NP_002652.2:p.Thr26Met
ENST00000564138.6:c.77C>T MANE Select	ENSP00000482457.1:p.Thr26Met
NM_002661.4:c.77C>T	NP_002652.2:p.Thr26Met
ENST00000359376.7:c.77C>T	ENSP00000352336.4:p.Thr26Met
ENST00000563193.2:c.77C>T	ENSP00000455533.2:p.Thr26Met
ENST00000564138.5:c.77C>T	ENSP00000482457.1:p.Thr26Met
ENST00000565054.5:c.77C>T	ENSP00000455956.1:p.Thr26Met
ENST00000567980.5:n.321C>T
ENST00000569929.5:n.207C>T
ENST00000697561.1:c.77C>T	ENSP00000513337.1:p.Thr26Met
ENST00000697562.1:c.77C>T	ENSP00000513338.1:p.Thr26Met
ENST00000697563.1:c.77C>T	ENSP00000513339.1:p.Thr26Met
ENST00000697564.1:c.77C>T	ENSP00000513340.1:p.Thr26Met
ENST00000697565.1:n.17C>T
ENST00000697581.1:c.77C>T	ENSP00000513346.1:p.Thr26Met
ENST00000697582.1:c.77C>T	ENSP00000513347.1:p.Thr26Met