Canonical Allele Identifier: CA2320550394

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679371C= , CM000681.2:g.6679371C=	GRCh38
NC_000019.9:g.6679382C= , CM000681.1:g.6679382C=	GRCh37
NC_000019.8:g.6630382C=	NCBI36
NG_009557.1:g.46281G= , LRG_27:g.46281G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2894+36G=
ENST00000695653.1:c.2455+36G=	ENSP00000512084.1:n.2455+36G=
ENST00000695654.1:c.3571+36G=	ENSP00000512085.1:n.3571+36G=
ENST00000695689.1:c.517+36G=	ENSP00000512101.1:n.517+36G=
ENST00000695690.1:n.1611+36G=
ENST00000695691.1:n.1407+36G=
ENST00000245907.11:c.4546+36G= MANE Select	ENSP00000245907.4:n.4546+36G=
ENST00000245907.10:c.4546+36G=	ENSP00000245907.4:n.4546+36G=
ENST00000599668.1:n.166+11G=
ENST00000599899.5:n.1505+36G=
ENST00000601008.1:c.242-1413G=	ENSP00000471384.1:n.242-1413G=
NM_000064.3:c.4546+36G=	NP_000055.2:n.4546+36G=
NM_000064.4:c.4546+36G= MANE Select	NP_000055.2:n.4546+36G=