Canonical Allele Identifier: CA1158487003

Gene: C1QB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22661034A= , CM000663.2:g.22661034A=	GRCh38
NC_000001.10:g.22987527A= , CM000663.1:g.22987527A=	GRCh37
NC_000001.9:g.22860114A=	NCBI36
NG_007283.1:g.12846A= , LRG_23:g.12846A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695754.1:c.404A=	ENSP00000512147.1:p.Asp135=
ENST00000695755.1:c.404A=	ENSP00000512148.1:p.Asp135=
ENST00000695756.1:c.404A=	ENSP00000512149.1:p.Asp135=
ENST00000695757.1:c.404A=	ENSP00000512150.1:p.Asp135=
ENST00000695758.1:c.430A=	ENSP00000512151.1:p.Thr144=
ENST00000695759.1:c.511A=	ENSP00000512152.1:p.Thr171=
ENST00000695760.1:c.482A=	ENSP00000512153.1:p.Asp161=
ENST00000695761.1:c.469A=	ENSP00000512154.1:p.Thr157=
ENST00000695762.1:c.395A=	ENSP00000512155.1:p.Asp132=
ENST00000695763.1:c.*573A=	ENSP00000512156.1:n.*573A=
ENST00000509305.6:c.404A= MANE Select	ENSP00000423689.1:p.Asp135=
ENST00000314933.6:c.410A=	ENSP00000313967.6:p.Asp137=
ENST00000432749.6:c.404A=	ENSP00000404606.2:p.Asp135=
ENST00000509305.5:c.404A=	ENSP00000423689.1:p.Asp135=
ENST00000510260.5:c.404A=	ENSP00000426317.1:p.Asp135=
NM_000491.3:c.410A= , LRG_23t1:c.410A=	NP_000482.3:p.Asp137=
XM_011542059.1:c.410A=	XP_011540361.1:p.Asp137=
NM_000491.4:c.410A=	NP_000482.3:p.Asp137=
XM_011542059.2:c.410A=	XP_011540361.1:p.Asp137=
NM_000491.5:c.410A=	NP_000482.3:p.Asp137=
NM_001371184.1:c.410A=	NP_001358113.1:p.Asp137=
NM_001371184.3:c.404A=	NP_001358113.2:p.Asp135=
NM_001378156.1:c.404A= MANE Select	NP_001365085.1:p.Asp135=