Canonical Allele Identifier: CA2320568366

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713993T= , CM000681.2:g.6713993T=	GRCh38
NC_000019.9:g.6714004T= , CM000681.1:g.6714004T=	GRCh37
NC_000019.8:g.6665004T=	NCBI36
NG_009557.1:g.11659A= , LRG_27:g.11659A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.649A=	ENSP00000512083.1:p.Arg217=
ENST00000245907.11:c.772A= MANE Select	ENSP00000245907.4:p.Arg258=
ENST00000245907.10:c.772A=	ENSP00000245907.4:p.Arg258=
ENST00000595577.1:n.276A=
NM_000064.3:c.772A=	NP_000055.2:p.Arg258=
NM_000064.4:c.772A= MANE Select	NP_000055.2:p.Arg258=