Canonical Allele Identifier: CA2320567852

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713276C= , CM000681.2:g.6713276C=	GRCh38
NC_000019.9:g.6713287C= , CM000681.1:g.6713287C=	GRCh37
NC_000019.8:g.6664287C=	NCBI36
NG_009557.1:g.12376G= , LRG_27:g.12376G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.793G=	ENSP00000512083.1:p.Val265=
ENST00000695654.1:c.40G=	ENSP00000512085.1:p.Val14=
ENST00000695692.1:n.240G=
ENST00000245907.11:c.916G= MANE Select	ENSP00000245907.4:p.Val306=
ENST00000245907.10:c.916G=	ENSP00000245907.4:p.Val306=
ENST00000594270.5:n.40G=
ENST00000595577.1:n.420G=
ENST00000597442.5:n.166G=
NM_000064.3:c.916G=	NP_000055.2:p.Val306=
NM_000064.4:c.916G= MANE Select	NP_000055.2:p.Val306=