Canonical Allele Identifier: CA2320559093

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697498C= , CM000681.2:g.6697498C=	GRCh38
NC_000019.9:g.6697509C= , CM000681.1:g.6697509C=	GRCh37
NC_000019.8:g.6648509C=	NCBI36
NG_009557.1:g.28154G= , LRG_27:g.28154G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.990G=
ENST00000695652.1:c.2519G=	ENSP00000512083.1:p.Arg840=
ENST00000695653.1:c.551G=	ENSP00000512084.1:p.Arg184=
ENST00000695654.1:c.1766G=	ENSP00000512085.1:p.Arg589=
ENST00000695655.1:c.1583G=	ENSP00000512086.1:n.1583G=
ENST00000695692.1:n.2006G=
ENST00000245907.11:c.2642G= MANE Select	ENSP00000245907.4:p.Arg881=
ENST00000245907.10:c.2642G=	ENSP00000245907.4:p.Arg881=
ENST00000594005.1:n.218G=
NM_000064.3:c.2642G=	NP_000055.2:p.Arg881=
NM_000064.4:c.2642G= MANE Select	NP_000055.2:p.Arg881=