Canonical Allele Identifier: CA1158487033

Gene: C1QB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22661130A= , CM000663.2:g.22661130A=	GRCh38
NC_000001.10:g.22987623A= , CM000663.1:g.22987623A=	GRCh37
NC_000001.9:g.22860210A=	NCBI36
NG_007283.1:g.12942A= , LRG_23:g.12942A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695754.1:c.500A=	ENSP00000512147.1:p.Tyr167=
ENST00000695755.1:c.500A=	ENSP00000512148.1:p.Tyr167=
ENST00000695756.1:c.500A=	ENSP00000512149.1:p.Tyr167=
ENST00000695757.1:c.500A=	ENSP00000512150.1:p.Tyr167=
ENST00000695758.1:c.*70A=	ENSP00000512151.1:n.*70A=
ENST00000695759.1:c.*70A=	ENSP00000512152.1:n.*70A=
ENST00000695760.1:c.578A=	ENSP00000512153.1:p.Tyr193=
ENST00000695761.1:c.*70A=	ENSP00000512154.1:n.*70A=
ENST00000695762.1:c.491A=	ENSP00000512155.1:p.Tyr164=
ENST00000695763.1:c.*669A=	ENSP00000512156.1:n.*669A=
ENST00000509305.6:c.500A= MANE Select	ENSP00000423689.1:p.Tyr167=
ENST00000314933.6:c.506A=	ENSP00000313967.6:p.Tyr169=
ENST00000432749.6:c.500A=	ENSP00000404606.2:p.Tyr167=
ENST00000509305.5:c.500A=	ENSP00000423689.1:p.Tyr167=
NM_000491.3:c.506A= , LRG_23t1:c.506A=	NP_000482.3:p.Tyr169=
XM_011542059.1:c.506A=	XP_011540361.1:p.Tyr169=
NM_000491.4:c.506A=	NP_000482.3:p.Tyr169=
XM_011542059.2:c.506A=	XP_011540361.1:p.Tyr169=
NM_000491.5:c.506A=	NP_000482.3:p.Tyr169=
NM_001371184.1:c.506A=	NP_001358113.1:p.Tyr169=
NM_001371184.3:c.500A=	NP_001358113.2:p.Tyr167=
NM_001378156.1:c.500A= MANE Select	NP_001365085.1:p.Tyr167=