Canonical Allele Identifier: CA2320567864

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713302G= , CM000681.2:g.6713302G=	GRCh38
NC_000019.9:g.6713313G= , CM000681.1:g.6713313G=	GRCh37
NC_000019.8:g.6664313G=	NCBI36
NG_009557.1:g.12350C= , LRG_27:g.12350C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.767C=	ENSP00000512083.1:p.Ser256=
ENST00000695654.1:c.14C=	ENSP00000512085.1:p.Ser5=
ENST00000695692.1:n.214C=
ENST00000245907.11:c.890C= MANE Select	ENSP00000245907.4:p.Ser297=
ENST00000245907.10:c.890C=	ENSP00000245907.4:p.Ser297=
ENST00000594270.5:n.14C=
ENST00000595577.1:n.394C=
ENST00000597442.5:n.140C=
NM_000064.3:c.890C=	NP_000055.2:p.Ser297=
NM_000064.4:c.890C= MANE Select	NP_000055.2:p.Ser297=