Canonical Allele Identifier: CA2320551642

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682200G= , CM000681.2:g.6682200G=	GRCh38
NC_000019.9:g.6682211G= , CM000681.1:g.6682211G=	GRCh37
NC_000019.8:g.6633211G=	NCBI36
NG_009557.1:g.43452C= , LRG_27:g.43452C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2550C=
ENST00000695653.1:c.2111C=	ENSP00000512084.1:p.Ser704=
ENST00000695654.1:c.3227C=	ENSP00000512085.1:p.Ser1076=
ENST00000695689.1:c.173C=	ENSP00000512101.1:n.173C=
ENST00000695690.1:n.393C=
ENST00000695691.1:n.393C=
ENST00000245907.11:c.4202C= MANE Select	ENSP00000245907.4:p.Ser1401=
ENST00000245907.10:c.4202C=	ENSP00000245907.4:p.Ser1401=
ENST00000596548.1:c.323C=	ENSP00000469744.1:p.Ser108=
ENST00000599899.5:n.1161C=
ENST00000601008.1:c.242-4242C=	ENSP00000471384.1:n.242-4242C=
NM_000064.3:c.4202C=	NP_000055.2:p.Ser1401=
NM_000064.4:c.4202C= MANE Select	NP_000055.2:p.Ser1401=