Canonical Allele Identifier: CA2320550409

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679416A= , CM000681.2:g.6679416A=	GRCh38
NC_000019.9:g.6679427A= , CM000681.1:g.6679427A=	GRCh37
NC_000019.8:g.6630427A=	NCBI36
NG_009557.1:g.46236T= , LRG_27:g.46236T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2885T=
ENST00000695653.1:c.2446T=	ENSP00000512084.1:p.Cys816=
ENST00000695654.1:c.3562T=	ENSP00000512085.1:p.Cys1188=
ENST00000695689.1:c.508T=	ENSP00000512101.1:n.508T=
ENST00000695690.1:n.1602T=
ENST00000695691.1:n.1398T=
ENST00000245907.11:c.4537T= MANE Select	ENSP00000245907.4:p.Cys1513=
ENST00000245907.10:c.4537T=	ENSP00000245907.4:p.Cys1513=
ENST00000599668.1:n.132T=
ENST00000599899.5:n.1496T=
ENST00000601008.1:c.242-1458T=	ENSP00000471384.1:n.242-1458T=
NM_000064.3:c.4537T=	NP_000055.2:p.Cys1513=
NM_000064.4:c.4537T= MANE Select	NP_000055.2:p.Cys1513=