Canonical Allele Identifier: CA2320559081

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697476G= , CM000681.2:g.6697476G=	GRCh38
NC_000019.9:g.6697487G= , CM000681.1:g.6697487G=	GRCh37
NC_000019.8:g.6648487G=	NCBI36
NG_009557.1:g.28176C= , LRG_27:g.28176C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1012C=
ENST00000695652.1:c.2541C=	ENSP00000512083.1:p.Ile847=
ENST00000695653.1:c.573C=	ENSP00000512084.1:p.Ile191=
ENST00000695654.1:c.1788C=	ENSP00000512085.1:p.Ile596=
ENST00000695655.1:c.1605C=	ENSP00000512086.1:n.1605C=
ENST00000695692.1:n.2028C=
ENST00000245907.11:c.2664C= MANE Select	ENSP00000245907.4:p.Ile888=
ENST00000245907.10:c.2664C=	ENSP00000245907.4:p.Ile888=
ENST00000594005.1:n.240C=
NM_000064.3:c.2664C=	NP_000055.2:p.Ile888=
NM_000064.4:c.2664C= MANE Select	NP_000055.2:p.Ile888=