Canonical Allele Identifier: CA2320559127

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697591G= , CM000681.2:g.6697591G=	GRCh38
NC_000019.9:g.6697602G= , CM000681.1:g.6697602G=	GRCh37
NC_000019.8:g.6648602G=	NCBI36
NG_009557.1:g.28061C= , LRG_27:g.28061C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.932-35C=
ENST00000695652.1:c.2461-35C=	ENSP00000512083.1:n.2461-35C=
ENST00000695653.1:c.493-35C=	ENSP00000512084.1:n.493-35C=
ENST00000695654.1:c.1708-35C=	ENSP00000512085.1:n.1708-35C=
ENST00000695655.1:c.1525-35C=	ENSP00000512086.1:n.1525-35C=
ENST00000695692.1:n.1948-35C=
ENST00000245907.11:c.2584-35C= MANE Select	ENSP00000245907.4:n.2584-35C=
ENST00000245907.10:c.2584-35C=	ENSP00000245907.4:n.2584-35C=
ENST00000594005.1:n.125C=
NM_000064.3:c.2584-35C=	NP_000055.2:n.2584-35C=
NM_000064.4:c.2584-35C= MANE Select	NP_000055.2:n.2584-35C=