Canonical Allele Identifier: CA1158487001

Gene: C1QB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22661028G= , CM000663.2:g.22661028G=	GRCh38
NC_000001.10:g.22987521G= , CM000663.1:g.22987521G=	GRCh37
NC_000001.9:g.22860108G=	NCBI36
NG_007283.1:g.12840G= , LRG_23:g.12840G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695754.1:c.398G=	ENSP00000512147.1:p.Arg133=
ENST00000695755.1:c.398G=	ENSP00000512148.1:p.Arg133=
ENST00000695756.1:c.398G=	ENSP00000512149.1:p.Arg133=
ENST00000695757.1:c.398G=	ENSP00000512150.1:p.Arg133=
ENST00000695758.1:c.424G=	ENSP00000512151.1:p.Ala142=
ENST00000695759.1:c.505G=	ENSP00000512152.1:p.Ala169=
ENST00000695760.1:c.476G=	ENSP00000512153.1:p.Arg159=
ENST00000695761.1:c.463G=	ENSP00000512154.1:p.Ala155=
ENST00000695762.1:c.389G=	ENSP00000512155.1:p.Arg130=
ENST00000695763.1:c.*567G=	ENSP00000512156.1:n.*567G=
ENST00000509305.6:c.398G= MANE Select	ENSP00000423689.1:p.Arg133=
ENST00000314933.6:c.404G=	ENSP00000313967.6:p.Arg135=
ENST00000432749.6:c.398G=	ENSP00000404606.2:p.Arg133=
ENST00000509305.5:c.398G=	ENSP00000423689.1:p.Arg133=
ENST00000510260.5:c.398G=	ENSP00000426317.1:p.Arg133=
NM_000491.3:c.404G= , LRG_23t1:c.404G=	NP_000482.3:p.Arg135=
XM_011542059.1:c.404G=	XP_011540361.1:p.Arg135=
NM_000491.4:c.404G=	NP_000482.3:p.Arg135=
XM_011542059.2:c.404G=	XP_011540361.1:p.Arg135=
NM_000491.5:c.404G=	NP_000482.3:p.Arg135=
NM_001371184.1:c.404G=	NP_001358113.1:p.Arg135=
NM_001371184.3:c.398G=	NP_001358113.2:p.Arg133=
NM_001378156.1:c.398G= MANE Select	NP_001365085.1:p.Arg133=