Canonical Allele Identifier: CA2320550198

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6678957C= , CM000681.2:g.6678957C=	GRCh38
NC_000019.9:g.6678968C= , CM000681.1:g.6678968C=	GRCh37
NC_000019.8:g.6629968C=	NCBI36
NG_009557.1:g.46695G= , LRG_27:g.46695G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2978+168G=
ENST00000695653.1:c.2539+168G=	ENSP00000512084.1:n.2539+168G=
ENST00000695654.1:c.3655+168G=	ENSP00000512085.1:n.3655+168G=
ENST00000695689.1:c.601+168G=	ENSP00000512101.1:n.601+168G=
ENST00000695690.1:n.1695+168G=
ENST00000695691.1:n.1491+168G=
ENST00000245907.11:c.4630+168G= MANE Select	ENSP00000245907.4:n.4630+168G=
ENST00000245907.10:c.4630+168G=	ENSP00000245907.4:n.4630+168G=
ENST00000599668.1:n.250+168G=
ENST00000599899.5:n.1589+168G=
ENST00000601008.1:c.242-999G=	ENSP00000471384.1:n.242-999G=
ENST00000602229.1:c.77+168G=
NM_000064.3:c.4630+168G=	NP_000055.2:n.4630+168G=
NM_000064.4:c.4630+168G= MANE Select	NP_000055.2:n.4630+168G=