Canonical Allele Identifier: CA2320559090

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697494G= , CM000681.2:g.6697494G=	GRCh38
NC_000019.9:g.6697505G= , CM000681.1:g.6697505G=	GRCh37
NC_000019.8:g.6648505G=	NCBI36
NG_009557.1:g.28158C= , LRG_27:g.28158C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.994C=
ENST00000695652.1:c.2523C=	ENSP00000512083.1:p.His841=
ENST00000695653.1:c.555C=	ENSP00000512084.1:p.His185=
ENST00000695654.1:c.1770C=	ENSP00000512085.1:p.His590=
ENST00000695655.1:c.1587C=	ENSP00000512086.1:n.1587C=
ENST00000695692.1:n.2010C=
ENST00000245907.11:c.2646C= MANE Select	ENSP00000245907.4:p.His882=
ENST00000245907.10:c.2646C=	ENSP00000245907.4:p.His882=
ENST00000594005.1:n.222C=
NM_000064.3:c.2646C=	NP_000055.2:p.His882=
NM_000064.4:c.2646C= MANE Select	NP_000055.2:p.His882=