Canonical Allele Identifier: CA2320550438

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679482G= , CM000681.2:g.6679482G=	GRCh38
NC_000019.9:g.6679493G= , CM000681.1:g.6679493G=	GRCh37
NC_000019.8:g.6630493G=	NCBI36
NG_009557.1:g.46170C= , LRG_27:g.46170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2819C=
ENST00000695653.1:c.2380C=	ENSP00000512084.1:p.Arg794=
ENST00000695654.1:c.3496C=	ENSP00000512085.1:p.Arg1166=
ENST00000695689.1:c.442C=	ENSP00000512101.1:n.442C=
ENST00000695690.1:n.1536C=
ENST00000695691.1:n.1332C=
ENST00000245907.11:c.4471C= MANE Select	ENSP00000245907.4:p.Arg1491=
ENST00000245907.10:c.4471C=	ENSP00000245907.4:p.Arg1491=
ENST00000599668.1:n.66C=
ENST00000599899.5:n.1430C=
ENST00000601008.1:c.242-1524C=	ENSP00000471384.1:n.242-1524C=
NM_000064.3:c.4471C=	NP_000055.2:p.Arg1491=
NM_000064.4:c.4471C= MANE Select	NP_000055.2:p.Arg1491=