Canonical Allele Identifier: CA2320553450

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686164T= , CM000681.2:g.6686164T=	GRCh38
NC_000019.9:g.6686175T= , CM000681.1:g.6686175T=	GRCh37
NC_000019.8:g.6637175T=	NCBI36
NG_009557.1:g.39488A= , LRG_27:g.39488A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2118A=
ENST00000695652.1:c.3647A=	ENSP00000512083.1:p.Asn1216=
ENST00000695653.1:c.1679A=	ENSP00000512084.1:p.Asn560=
ENST00000695654.1:c.2795A=	ENSP00000512085.1:p.Asn932=
ENST00000695655.1:c.2711A=	ENSP00000512086.1:n.2711A=
ENST00000695692.1:n.3134A=
ENST00000245907.11:c.3770A= MANE Select	ENSP00000245907.4:p.Asn1257=
ENST00000245907.10:c.3770A=	ENSP00000245907.4:p.Asn1257=
ENST00000596238.1:n.213A=
ENST00000601008.1:c.241+582A=	ENSP00000471384.1:n.241+582A=
NM_000064.3:c.3770A=	NP_000055.2:p.Asn1257=
NM_000064.4:c.3770A= MANE Select	NP_000055.2:p.Asn1257=