Canonical Allele Identifier: CA2320553459

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686183G= , CM000681.2:g.6686183G=	GRCh38
NC_000019.9:g.6686194G= , CM000681.1:g.6686194G=	GRCh37
NC_000019.8:g.6637194G=	NCBI36
NG_009557.1:g.39469C= , LRG_27:g.39469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2099C=
ENST00000695652.1:c.3628C=	ENSP00000512083.1:p.Pro1210=
ENST00000695653.1:c.1660C=	ENSP00000512084.1:p.Pro554=
ENST00000695654.1:c.2776C=	ENSP00000512085.1:p.Pro926=
ENST00000695655.1:c.2692C=	ENSP00000512086.1:n.2692C=
ENST00000695692.1:n.3115C=
ENST00000245907.11:c.3751C= MANE Select	ENSP00000245907.4:p.Pro1251=
ENST00000245907.10:c.3751C=	ENSP00000245907.4:p.Pro1251=
ENST00000596238.1:n.194C=
ENST00000601008.1:c.241+563C=	ENSP00000471384.1:n.241+563C=
NM_000064.3:c.3751C=	NP_000055.2:p.Pro1251=
NM_000064.4:c.3751C= MANE Select	NP_000055.2:p.Pro1251=