Canonical Allele Identifier: CA2320567863

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713301C= , CM000681.2:g.6713301C=	GRCh38
NC_000019.9:g.6713312C= , CM000681.1:g.6713312C=	GRCh37
NC_000019.8:g.6664312C=	NCBI36
NG_009557.1:g.12351G= , LRG_27:g.12351G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.768G=	ENSP00000512083.1:p.Ser256=
ENST00000695654.1:c.15G=	ENSP00000512085.1:p.Ser5=
ENST00000695692.1:n.215G=
ENST00000245907.11:c.891G= MANE Select	ENSP00000245907.4:p.Ser297=
ENST00000245907.10:c.891G=	ENSP00000245907.4:p.Ser297=
ENST00000594270.5:n.15G=
ENST00000595577.1:n.395G=
ENST00000597442.5:n.141G=
NM_000064.3:c.891G=	NP_000055.2:p.Ser297=
NM_000064.4:c.891G= MANE Select	NP_000055.2:p.Ser297=