Canonical Allele Identifier: CA2320550440

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679486A= , CM000681.2:g.6679486A=	GRCh38
NC_000019.9:g.6679497A= , CM000681.1:g.6679497A=	GRCh37
NC_000019.8:g.6630497A=	NCBI36
NG_009557.1:g.46166T= , LRG_27:g.46166T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2815T=
ENST00000695653.1:c.2376T=	ENSP00000512084.1:p.Cys792=
ENST00000695654.1:c.3492T=	ENSP00000512085.1:p.Cys1164=
ENST00000695689.1:c.438T=	ENSP00000512101.1:n.438T=
ENST00000695690.1:n.1532T=
ENST00000695691.1:n.1328T=
ENST00000245907.11:c.4467T= MANE Select	ENSP00000245907.4:p.Cys1489=
ENST00000245907.10:c.4467T=	ENSP00000245907.4:p.Cys1489=
ENST00000599668.1:n.62T=
ENST00000599899.5:n.1426T=
ENST00000601008.1:c.242-1528T=	ENSP00000471384.1:n.242-1528T=
NM_000064.3:c.4467T=	NP_000055.2:p.Cys1489=
NM_000064.4:c.4467T= MANE Select	NP_000055.2:p.Cys1489=