Canonical Allele Identifier: CA2320553490

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686263C= , CM000681.2:g.6686263C=	GRCh38
NC_000019.9:g.6686274C= , CM000681.1:g.6686274C=	GRCh37
NC_000019.8:g.6637274C=	NCBI36
NG_009557.1:g.39389G= , LRG_27:g.39389G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2019G=
ENST00000695652.1:c.3548G=	ENSP00000512083.1:p.Gly1183=
ENST00000695653.1:c.1580G=	ENSP00000512084.1:p.Gly527=
ENST00000695654.1:c.2696G=	ENSP00000512085.1:p.Gly899=
ENST00000695655.1:c.2612G=	ENSP00000512086.1:n.2612G=
ENST00000695692.1:n.3035G=
ENST00000245907.11:c.3671G= MANE Select	ENSP00000245907.4:p.Gly1224=
ENST00000245907.10:c.3671G=	ENSP00000245907.4:p.Gly1224=
ENST00000596238.1:n.114G=
ENST00000601008.1:c.241+483G=	ENSP00000471384.1:n.241+483G=
NM_000064.3:c.3671G=	NP_000055.2:p.Gly1224=
NM_000064.4:c.3671G= MANE Select	NP_000055.2:p.Gly1224=