Canonical Allele Identifier: CA2320553463

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686195C= , CM000681.2:g.6686195C=	GRCh38
NC_000019.9:g.6686206C= , CM000681.1:g.6686206C=	GRCh37
NC_000019.8:g.6637206C=	NCBI36
NG_009557.1:g.39457G= , LRG_27:g.39457G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2087G=
ENST00000695652.1:c.3616G=	ENSP00000512083.1:p.Asp1206=
ENST00000695653.1:c.1648G=	ENSP00000512084.1:p.Asp550=
ENST00000695654.1:c.2764G=	ENSP00000512085.1:p.Asp922=
ENST00000695655.1:c.2680G=	ENSP00000512086.1:n.2680G=
ENST00000695692.1:n.3103G=
ENST00000245907.11:c.3739G= MANE Select	ENSP00000245907.4:p.Asp1247=
ENST00000245907.10:c.3739G=	ENSP00000245907.4:p.Asp1247=
ENST00000596238.1:n.182G=
ENST00000601008.1:c.241+551G=	ENSP00000471384.1:n.241+551G=
NM_000064.3:c.3739G=	NP_000055.2:p.Asp1247=
NM_000064.4:c.3739G= MANE Select	NP_000055.2:p.Asp1247=