Canonical Allele Identifier: CA1143368335

Gene: C1QB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22661031G= , CM000663.2:g.22661031G=	GRCh38
NC_000001.10:g.22987524G= , CM000663.1:g.22987524G=	GRCh37
NC_000001.9:g.22860111G=	NCBI36
NG_007283.1:g.12843G= , LRG_23:g.12843G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695754.1:c.401G=	ENSP00000512147.1:p.Arg134=
ENST00000695755.1:c.401G=	ENSP00000512148.1:p.Arg134=
ENST00000695756.1:c.401G=	ENSP00000512149.1:p.Arg134=
ENST00000695757.1:c.401G=	ENSP00000512150.1:p.Arg134=
ENST00000695758.1:c.427G=	ENSP00000512151.1:p.Gly143=
ENST00000695759.1:c.508G=	ENSP00000512152.1:p.Gly170=
ENST00000695760.1:c.479G=	ENSP00000512153.1:p.Arg160=
ENST00000695761.1:c.466G=	ENSP00000512154.1:p.Gly156=
ENST00000695762.1:c.392G=	ENSP00000512155.1:p.Arg131=
ENST00000695763.1:c.*570G=	ENSP00000512156.1:n.*570G=
ENST00000509305.6:c.401G= MANE Select	ENSP00000423689.1:p.Arg134=
ENST00000314933.6:c.407G=	ENSP00000313967.6:p.Arg136=
ENST00000432749.6:c.401G=	ENSP00000404606.2:p.Arg134=
ENST00000509305.5:c.401G=	ENSP00000423689.1:p.Arg134=
ENST00000510260.5:c.401G=	ENSP00000426317.1:p.Arg134=
NM_000491.3:c.407G= , LRG_23t1:c.407G=	NP_000482.3:p.Arg136=
XM_011542059.1:c.407G=	XP_011540361.1:p.Arg136=
NM_000491.4:c.407G=	NP_000482.3:p.Arg136=
XM_011542059.2:c.407G=	XP_011540361.1:p.Arg136=
NM_000491.5:c.407G=	NP_000482.3:p.Arg136=
NM_001371184.1:c.407G=	NP_001358113.1:p.Arg136=
NM_001371184.3:c.401G=	NP_001358113.2:p.Arg134=
NM_001378156.1:c.401G= MANE Select	NP_001365085.1:p.Arg134=