Canonical Allele Identifier: CA2320566003

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709912G= , CM000681.2:g.6709912G=	GRCh38
NC_000019.9:g.6709923G= , CM000681.1:g.6709923G=	GRCh37
NC_000019.8:g.6660923G=	NCBI36
NG_009557.1:g.15740C= , LRG_27:g.15740C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-70C=	ENSP00000512083.1:n.1564-70C=
ENST00000695654.1:c.811-70C=	ENSP00000512085.1:n.811-70C=
ENST00000695655.1:c.592-34C=	ENSP00000512086.1:n.592-34C=
ENST00000695692.1:n.1051-70C=
ENST00000245907.11:c.1687-70C= MANE Select	ENSP00000245907.4:n.1687-70C=
ENST00000245907.10:c.1687-70C=	ENSP00000245907.4:n.1687-70C=
ENST00000600763.1:n.320-70C=
NM_000064.3:c.1687-70C=	NP_000055.2:n.1687-70C=
NM_000064.4:c.1687-70C= MANE Select	NP_000055.2:n.1687-70C=