Canonical Allele Identifier: CA2320553492

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686267G= , CM000681.2:g.6686267G=	GRCh38
NC_000019.9:g.6686278G= , CM000681.1:g.6686278G=	GRCh37
NC_000019.8:g.6637278G=	NCBI36
NG_009557.1:g.39385C= , LRG_27:g.39385C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2015C=
ENST00000695652.1:c.3544C=	ENSP00000512083.1:p.Pro1182=
ENST00000695653.1:c.1576C=	ENSP00000512084.1:p.Pro526=
ENST00000695654.1:c.2692C=	ENSP00000512085.1:p.Pro898=
ENST00000695655.1:c.2608C=	ENSP00000512086.1:n.2608C=
ENST00000695692.1:n.3031C=
ENST00000245907.11:c.3667C= MANE Select	ENSP00000245907.4:p.Pro1223=
ENST00000245907.10:c.3667C=	ENSP00000245907.4:p.Pro1223=
ENST00000596238.1:n.110C=
ENST00000601008.1:c.241+479C=	ENSP00000471384.1:n.241+479C=
NM_000064.3:c.3667C=	NP_000055.2:p.Pro1223=
NM_000064.4:c.3667C= MANE Select	NP_000055.2:p.Pro1223=