Canonical Allele Identifier: CA2320559178

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697687C= , CM000681.2:g.6697687C=	GRCh38
NC_000019.9:g.6697698C= , CM000681.1:g.6697698C=	GRCh37
NC_000019.8:g.6648698C=	NCBI36
NG_009557.1:g.27965G= , LRG_27:g.27965G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.896G=
ENST00000695652.1:c.2425G=	ENSP00000512083.1:p.Val809=
ENST00000695653.1:c.457G=	ENSP00000512084.1:p.Val153=
ENST00000695654.1:c.1672G=	ENSP00000512085.1:p.Val558=
ENST00000695655.1:c.1489G=	ENSP00000512086.1:n.1489G=
ENST00000695692.1:n.1912G=
ENST00000245907.11:c.2548G= MANE Select	ENSP00000245907.4:p.Val850=
ENST00000245907.10:c.2548G=	ENSP00000245907.4:p.Val850=
ENST00000594005.1:n.29G=
ENST00000602053.1:n.596G=
NM_000064.3:c.2548G=	NP_000055.2:p.Val850=
NM_000064.4:c.2548G= MANE Select	NP_000055.2:p.Val850=