Canonical Allele Identifier: CA2320553443

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686141C= , CM000681.2:g.6686141C=	GRCh38
NC_000019.9:g.6686152C= , CM000681.1:g.6686152C=	GRCh37
NC_000019.8:g.6637152C=	NCBI36
NG_009557.1:g.39511G= , LRG_27:g.39511G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2141G=
ENST00000695652.1:c.3670G=	ENSP00000512083.1:p.Gly1224=
ENST00000695653.1:c.1702G=	ENSP00000512084.1:p.Gly568=
ENST00000695654.1:c.2818G=	ENSP00000512085.1:p.Gly940=
ENST00000695655.1:c.2734G=	ENSP00000512086.1:n.2734G=
ENST00000695692.1:n.3157G=
ENST00000245907.11:c.3793G= MANE Select	ENSP00000245907.4:p.Gly1265=
ENST00000245907.10:c.3793G=	ENSP00000245907.4:p.Gly1265=
ENST00000596238.1:n.236G=
ENST00000601008.1:c.241+605G=	ENSP00000471384.1:n.241+605G=
NM_000064.3:c.3793G=	NP_000055.2:p.Gly1265=
NM_000064.4:c.3793G= MANE Select	NP_000055.2:p.Gly1265=