Canonical Allele Identifier: CA2320553481

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686238G= , CM000681.2:g.6686238G=	GRCh38
NC_000019.9:g.6686249G= , CM000681.1:g.6686249G=	GRCh37
NC_000019.8:g.6637249G=	NCBI36
NG_009557.1:g.39414C= , LRG_27:g.39414C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2044C=
ENST00000695652.1:c.3573C=	ENSP00000512083.1:p.Ala1191=
ENST00000695653.1:c.1605C=	ENSP00000512084.1:p.Ala535=
ENST00000695654.1:c.2721C=	ENSP00000512085.1:p.Ala907=
ENST00000695655.1:c.2637C=	ENSP00000512086.1:n.2637C=
ENST00000695692.1:n.3060C=
ENST00000245907.11:c.3696C= MANE Select	ENSP00000245907.4:p.Ala1232=
ENST00000245907.10:c.3696C=	ENSP00000245907.4:p.Ala1232=
ENST00000596238.1:n.139C=
ENST00000601008.1:c.241+508C=	ENSP00000471384.1:n.241+508C=
NM_000064.3:c.3696C=	NP_000055.2:p.Ala1232=
NM_000064.4:c.3696C= MANE Select	NP_000055.2:p.Ala1232=