Canonical Allele Identifier: CA2320551540

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681971A= , CM000681.2:g.6681971A=	GRCh38
NC_000019.9:g.6681982A= , CM000681.1:g.6681982A=	GRCh37
NC_000019.8:g.6632982A=	NCBI36
NG_009557.1:g.43681T= , LRG_27:g.43681T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2668T=
ENST00000695653.1:c.2229T=	ENSP00000512084.1:p.Asp743=
ENST00000695654.1:c.3345T=	ENSP00000512085.1:p.Asp1115=
ENST00000695689.1:c.291T=	ENSP00000512101.1:n.291T=
ENST00000695690.1:n.511T=
ENST00000695691.1:n.511T=
ENST00000245907.11:c.4320T= MANE Select	ENSP00000245907.4:p.Asp1440=
ENST00000245907.10:c.4320T=	ENSP00000245907.4:p.Asp1440=
ENST00000596548.1:c.441T=	ENSP00000469744.1:p.Asp147=
ENST00000599899.5:n.1279T=
ENST00000601008.1:c.242-4013T=	ENSP00000471384.1:n.242-4013T=
NM_000064.3:c.4320T=	NP_000055.2:p.Asp1440=
NM_000064.4:c.4320T= MANE Select	NP_000055.2:p.Asp1440=