Canonical Allele Identifier: CA2320568472

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714225G= , CM000681.2:g.6714225G=	GRCh38
NC_000019.9:g.6714236G= , CM000681.1:g.6714236G=	GRCh37
NC_000019.8:g.6665236G=	NCBI36
NG_009557.1:g.11427C= , LRG_27:g.11427C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.500C=	ENSP00000512083.1:p.Ala167=
ENST00000245907.11:c.623C= MANE Select	ENSP00000245907.4:p.Ala208=
ENST00000245907.10:c.623C=	ENSP00000245907.4:p.Ala208=
ENST00000595577.1:n.127C=
NM_000064.3:c.623C=	NP_000055.2:p.Ala208=
NM_000064.4:c.623C= MANE Select	NP_000055.2:p.Ala208=