Canonical Allele Identifier: CA2320550291

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679193T= , CM000681.2:g.6679193T=	GRCh38
NC_000019.9:g.6679204T= , CM000681.1:g.6679204T=	GRCh37
NC_000019.8:g.6630204T=	NCBI36
NG_009557.1:g.46459A= , LRG_27:g.46459A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2910A=
ENST00000695653.1:c.2471A=	ENSP00000512084.1:p.Gln824=
ENST00000695654.1:c.3587A=	ENSP00000512085.1:p.Gln1196=
ENST00000695689.1:c.533A=	ENSP00000512101.1:n.533A=
ENST00000695690.1:n.1627A=
ENST00000695691.1:n.1423A=
ENST00000245907.11:c.4562A= MANE Select	ENSP00000245907.4:p.Gln1521=
ENST00000245907.10:c.4562A=	ENSP00000245907.4:p.Gln1521=
ENST00000599668.1:n.182A=
ENST00000599899.5:n.1521A=
ENST00000601008.1:c.242-1235A=	ENSP00000471384.1:n.242-1235A=
ENST00000602229.1:c.9A=
NM_000064.3:c.4562A=	NP_000055.2:p.Gln1521=
NM_000064.4:c.4562A= MANE Select	NP_000055.2:p.Gln1521=