Canonical Allele Identifier: CA2320550412

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679419G= , CM000681.2:g.6679419G=	GRCh38
NC_000019.9:g.6679430G= , CM000681.1:g.6679430G=	GRCh37
NC_000019.8:g.6630430G=	NCBI36
NG_009557.1:g.46233C= , LRG_27:g.46233C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2882C=
ENST00000695653.1:c.2443C=	ENSP00000512084.1:p.Arg815=
ENST00000695654.1:c.3559C=	ENSP00000512085.1:p.Arg1187=
ENST00000695689.1:c.505C=	ENSP00000512101.1:n.505C=
ENST00000695690.1:n.1599C=
ENST00000695691.1:n.1395C=
ENST00000245907.11:c.4534C= MANE Select	ENSP00000245907.4:p.Arg1512=
ENST00000245907.10:c.4534C=	ENSP00000245907.4:p.Arg1512=
ENST00000599668.1:n.129C=
ENST00000599899.5:n.1493C=
ENST00000601008.1:c.242-1461C=	ENSP00000471384.1:n.242-1461C=
NM_000064.3:c.4534C=	NP_000055.2:p.Arg1512=
NM_000064.4:c.4534C= MANE Select	NP_000055.2:p.Arg1512=