Canonical Allele Identifier: CA2320559047

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697395A= , CM000681.2:g.6697395A=	GRCh38
NC_000019.9:g.6697406A= , CM000681.1:g.6697406A=	GRCh37
NC_000019.8:g.6648406A=	NCBI36
NG_009557.1:g.28257T= , LRG_27:g.28257T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1093T=
ENST00000695652.1:c.2622T=	ENSP00000512083.1:p.Ala874=
ENST00000695653.1:c.654T=	ENSP00000512084.1:p.Ala218=
ENST00000695654.1:c.1869T=	ENSP00000512085.1:p.Ala623=
ENST00000695655.1:c.1686T=	ENSP00000512086.1:n.1686T=
ENST00000695692.1:n.2109T=
ENST00000245907.11:c.2745T= MANE Select	ENSP00000245907.4:p.Ala915=
ENST00000245907.10:c.2745T=	ENSP00000245907.4:p.Ala915=
ENST00000594005.1:n.321T=
NM_000064.3:c.2745T=	NP_000055.2:p.Ala915=
NM_000064.4:c.2745T= MANE Select	NP_000055.2:p.Ala915=