Canonical Allele Identifier: CA2320559068

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697455G= , CM000681.2:g.6697455G=	GRCh38
NC_000019.9:g.6697466G= , CM000681.1:g.6697466G=	GRCh37
NC_000019.8:g.6648466G=	NCBI36
NG_009557.1:g.28197C= , LRG_27:g.28197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1033C=
ENST00000695652.1:c.2562C=	ENSP00000512083.1:p.Ser854=
ENST00000695653.1:c.594C=	ENSP00000512084.1:p.Ser198=
ENST00000695654.1:c.1809C=	ENSP00000512085.1:p.Ser603=
ENST00000695655.1:c.1626C=	ENSP00000512086.1:n.1626C=
ENST00000695692.1:n.2049C=
ENST00000245907.11:c.2685C= MANE Select	ENSP00000245907.4:p.Ser895=
ENST00000245907.10:c.2685C=	ENSP00000245907.4:p.Ser895=
ENST00000594005.1:n.261C=
NM_000064.3:c.2685C=	NP_000055.2:p.Ser895=
NM_000064.4:c.2685C= MANE Select	NP_000055.2:p.Ser895=