Canonical Allele Identifier: CA338947604

Gene: C1QB

Linked Data

• MyVariant Identifiers: chr1:g.22987565A>C (hg19) ; chr1:g.22661072A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22661072A>C , CM000663.2:g.22661072A>C	GRCh38
NC_000001.10:g.22987565A>C , CM000663.1:g.22987565A>C	GRCh37
NC_000001.9:g.22860152A>C	NCBI36
NG_007283.1:g.12884A>C , LRG_23:g.12884A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695754.1:c.442A>C	ENSP00000512147.1:p.Asn148His
ENST00000695755.1:c.442A>C	ENSP00000512148.1:p.Asn148His
ENST00000695756.1:c.442A>C	ENSP00000512149.1:p.Asn148His
ENST00000695757.1:c.442A>C	ENSP00000512150.1:p.Asn148His
ENST00000695758.1:c.*12A>C	ENSP00000512151.1:n.*12A>C
ENST00000695759.1:c.*12A>C	ENSP00000512152.1:n.*12A>C
ENST00000695760.1:c.520A>C	ENSP00000512153.1:p.Asn174His
ENST00000695761.1:c.*12A>C	ENSP00000512154.1:n.*12A>C
ENST00000695762.1:c.433A>C	ENSP00000512155.1:p.Asn145His
ENST00000695763.1:c.*611A>C	ENSP00000512156.1:n.*611A>C
ENST00000509305.6:c.442A>C MANE Select	ENSP00000423689.1:p.Asn148His
ENST00000314933.6:c.448A>C	ENSP00000313967.6:p.Asn150His
ENST00000432749.6:c.442A>C	ENSP00000404606.2:p.Asn148His
ENST00000509305.5:c.442A>C	ENSP00000423689.1:p.Asn148His
ENST00000510260.5:c.442A>C	ENSP00000426317.1:p.Asn148His
NM_000491.3:c.448A>C , LRG_23t1:c.448A>C	NP_000482.3:p.Asn150His
XM_011542059.1:c.448A>C	XP_011540361.1:p.Asn150His
NM_000491.4:c.448A>C	NP_000482.3:p.Asn150His
XM_011542059.2:c.448A>C	XP_011540361.1:p.Asn150His
NM_000491.5:c.448A>C	NP_000482.3:p.Asn150His
NM_001371184.1:c.448A>C	NP_001358113.1:p.Asn150His
NM_001371184.3:c.442A>C	NP_001358113.2:p.Asn148His
NM_001378156.1:c.442A>C MANE Select	NP_001365085.1:p.Asn148His