Canonical Allele Identifier: CA2320550426

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679450C= , CM000681.2:g.6679450C=	GRCh38
NC_000019.9:g.6679461C= , CM000681.1:g.6679461C=	GRCh37
NC_000019.8:g.6630461C=	NCBI36
NG_009557.1:g.46202G= , LRG_27:g.46202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2851G=
ENST00000695653.1:c.2412G=	ENSP00000512084.1:p.Lys804=
ENST00000695654.1:c.3528G=	ENSP00000512085.1:p.Lys1176=
ENST00000695689.1:c.474G=	ENSP00000512101.1:n.474G=
ENST00000695690.1:n.1568G=
ENST00000695691.1:n.1364G=
ENST00000245907.11:c.4503G= MANE Select	ENSP00000245907.4:p.Lys1501=
ENST00000245907.10:c.4503G=	ENSP00000245907.4:p.Lys1501=
ENST00000599668.1:n.98G=
ENST00000599899.5:n.1462G=
ENST00000601008.1:c.242-1492G=	ENSP00000471384.1:n.242-1492G=
NM_000064.3:c.4503G=	NP_000055.2:p.Lys1501=
NM_000064.4:c.4503G= MANE Select	NP_000055.2:p.Lys1501=