Canonical Allele Identifier: CA2320559076

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697470G= , CM000681.2:g.6697470G=	GRCh38
NC_000019.9:g.6697481G= , CM000681.1:g.6697481G=	GRCh37
NC_000019.8:g.6648481G=	NCBI36
NG_009557.1:g.28182C= , LRG_27:g.28182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1018C=
ENST00000695652.1:c.2547C=	ENSP00000512083.1:p.Pro849=
ENST00000695653.1:c.579C=	ENSP00000512084.1:p.Pro193=
ENST00000695654.1:c.1794C=	ENSP00000512085.1:p.Pro598=
ENST00000695655.1:c.1611C=	ENSP00000512086.1:n.1611C=
ENST00000695692.1:n.2034C=
ENST00000245907.11:c.2670C= MANE Select	ENSP00000245907.4:p.Pro890=
ENST00000245907.10:c.2670C=	ENSP00000245907.4:p.Pro890=
ENST00000594005.1:n.246C=
NM_000064.3:c.2670C=	NP_000055.2:p.Pro890=
NM_000064.4:c.2670C= MANE Select	NP_000055.2:p.Pro890=