Canonical Allele Identifier: CA2320553458

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686182G= , CM000681.2:g.6686182G=	GRCh38
NC_000019.9:g.6686193G= , CM000681.1:g.6686193G=	GRCh37
NC_000019.8:g.6637193G=	NCBI36
NG_009557.1:g.39470C= , LRG_27:g.39470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2100C=
ENST00000695652.1:c.3629C=	ENSP00000512083.1:p.Pro1210=
ENST00000695653.1:c.1661C=	ENSP00000512084.1:p.Pro554=
ENST00000695654.1:c.2777C=	ENSP00000512085.1:p.Pro926=
ENST00000695655.1:c.2693C=	ENSP00000512086.1:n.2693C=
ENST00000695692.1:n.3116C=
ENST00000245907.11:c.3752C= MANE Select	ENSP00000245907.4:p.Pro1251=
ENST00000245907.10:c.3752C=	ENSP00000245907.4:p.Pro1251=
ENST00000596238.1:n.195C=
ENST00000601008.1:c.241+564C=	ENSP00000471384.1:n.241+564C=
NM_000064.3:c.3752C=	NP_000055.2:p.Pro1251=
NM_000064.4:c.3752C= MANE Select	NP_000055.2:p.Pro1251=