Canonical Allele Identifier: CA2320550337

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679260T= , CM000681.2:g.6679260T=	GRCh38
NC_000019.9:g.6679271T= , CM000681.1:g.6679271T=	GRCh37
NC_000019.8:g.6630271T=	NCBI36
NG_009557.1:g.46392A= , LRG_27:g.46392A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2895-52A=
ENST00000695653.1:c.2456-52A=	ENSP00000512084.1:n.2456-52A=
ENST00000695654.1:c.3572-52A=	ENSP00000512085.1:n.3572-52A=
ENST00000695689.1:c.518-52A=	ENSP00000512101.1:n.518-52A=
ENST00000695690.1:n.1612-52A=
ENST00000695691.1:n.1408-52A=
ENST00000245907.11:c.4547-52A= MANE Select	ENSP00000245907.4:n.4547-52A=
ENST00000245907.10:c.4547-52A=	ENSP00000245907.4:n.4547-52A=
ENST00000599668.1:n.167-52A=
ENST00000599899.5:n.1506-52A=
ENST00000601008.1:c.242-1302A=	ENSP00000471384.1:n.242-1302A=
NM_000064.3:c.4547-52A=	NP_000055.2:n.4547-52A=
NM_000064.4:c.4547-52A= MANE Select	NP_000055.2:n.4547-52A=