Canonical Allele Identifier: CA2320553469

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686208C= , CM000681.2:g.6686208C=	GRCh38
NC_000019.9:g.6686219C= , CM000681.1:g.6686219C=	GRCh37
NC_000019.8:g.6637219C=	NCBI36
NG_009557.1:g.39444G= , LRG_27:g.39444G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2074G=
ENST00000695652.1:c.3603G=	ENSP00000512083.1:p.Gln1201=
ENST00000695653.1:c.1635G=	ENSP00000512084.1:p.Gln545=
ENST00000695654.1:c.2751G=	ENSP00000512085.1:p.Gln917=
ENST00000695655.1:c.2667G=	ENSP00000512086.1:n.2667G=
ENST00000695692.1:n.3090G=
ENST00000245907.11:c.3726G= MANE Select	ENSP00000245907.4:p.Gln1242=
ENST00000245907.10:c.3726G=	ENSP00000245907.4:p.Gln1242=
ENST00000596238.1:n.169G=
ENST00000601008.1:c.241+538G=	ENSP00000471384.1:n.241+538G=
NM_000064.3:c.3726G=	NP_000055.2:p.Gln1242=
NM_000064.4:c.3726G= MANE Select	NP_000055.2:p.Gln1242=