Canonical Allele Identifier: CA2320559167

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697654T= , CM000681.2:g.6697654T=	GRCh38
NC_000019.9:g.6697665T= , CM000681.1:g.6697665T=	GRCh37
NC_000019.8:g.6648665T=	NCBI36
NG_009557.1:g.27998A= , LRG_27:g.27998A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.929A=
ENST00000695652.1:c.2458A=	ENSP00000512083.1:p.Lys820=
ENST00000695653.1:c.490A=	ENSP00000512084.1:p.Lys164=
ENST00000695654.1:c.1705A=	ENSP00000512085.1:p.Lys569=
ENST00000695655.1:c.1522A=	ENSP00000512086.1:n.1522A=
ENST00000695692.1:n.1945A=
ENST00000245907.11:c.2581A= MANE Select	ENSP00000245907.4:p.Lys861=
ENST00000245907.10:c.2581A=	ENSP00000245907.4:p.Lys861=
ENST00000594005.1:n.62A=
NM_000064.3:c.2581A=	NP_000055.2:p.Lys861=
NM_000064.4:c.2581A= MANE Select	NP_000055.2:p.Lys861=