Canonical Allele Identifier: CA2320550422

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679441C= , CM000681.2:g.6679441C=	GRCh38
NC_000019.9:g.6679452C= , CM000681.1:g.6679452C=	GRCh37
NC_000019.8:g.6630452C=	NCBI36
NG_009557.1:g.46211G= , LRG_27:g.46211G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2860G=
ENST00000695653.1:c.2421G=	ENSP00000512084.1:p.Lys807=
ENST00000695654.1:c.3537G=	ENSP00000512085.1:p.Lys1179=
ENST00000695689.1:c.483G=	ENSP00000512101.1:n.483G=
ENST00000695690.1:n.1577G=
ENST00000695691.1:n.1373G=
ENST00000245907.11:c.4512G= MANE Select	ENSP00000245907.4:p.Lys1504=
ENST00000245907.10:c.4512G=	ENSP00000245907.4:p.Lys1504=
ENST00000599668.1:n.107G=
ENST00000599899.5:n.1471G=
ENST00000601008.1:c.242-1483G=	ENSP00000471384.1:n.242-1483G=
NM_000064.3:c.4512G=	NP_000055.2:p.Lys1504=
NM_000064.4:c.4512G= MANE Select	NP_000055.2:p.Lys1504=