Canonical Allele Identifier: CA2320566096

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710023G= , CM000681.2:g.6710023G=	GRCh38
NC_000019.9:g.6710034G= , CM000681.1:g.6710034G=	GRCh37
NC_000019.8:g.6661034G=	NCBI36
NG_009557.1:g.15629C= , LRG_27:g.15629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-181C=	ENSP00000512083.1:n.1564-181C=
ENST00000695654.1:c.811-181C=	ENSP00000512085.1:n.811-181C=
ENST00000695655.1:c.592-145C=	ENSP00000512086.1:n.592-145C=
ENST00000695692.1:n.1051-181C=
ENST00000245907.11:c.1687-181C= MANE Select	ENSP00000245907.4:n.1687-181C=
ENST00000245907.10:c.1687-181C=	ENSP00000245907.4:n.1687-181C=
ENST00000600763.1:n.320-181C=
NM_000064.3:c.1687-181C=	NP_000055.2:n.1687-181C=
NM_000064.4:c.1687-181C= MANE Select	NP_000055.2:n.1687-181C=