Canonical Allele Identifier: CA2320565937

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709755G= , CM000681.2:g.6709755G=	GRCh38
NC_000019.9:g.6709766G= , CM000681.1:g.6709766G=	GRCh37
NC_000019.8:g.6660766G=	NCBI36
NG_009557.1:g.15897C= , LRG_27:g.15897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1651C=	ENSP00000512083.1:p.Arg551=
ENST00000695654.1:c.898C=	ENSP00000512085.1:p.Arg300=
ENST00000695655.1:c.715C=	ENSP00000512086.1:n.715C=
ENST00000695692.1:n.1138C=
ENST00000245907.11:c.1774C= MANE Select	ENSP00000245907.4:p.Arg592=
ENST00000245907.10:c.1774C=	ENSP00000245907.4:p.Arg592=
NM_000064.3:c.1774C=	NP_000055.2:p.Arg592=
NM_000064.4:c.1774C= MANE Select	NP_000055.2:p.Arg592=