Canonical Allele Identifier: CA2320559173

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697673G= , CM000681.2:g.6697673G=	GRCh38
NC_000019.9:g.6697684G= , CM000681.1:g.6697684G=	GRCh37
NC_000019.8:g.6648684G=	NCBI36
NG_009557.1:g.27979C= , LRG_27:g.27979C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.910C=
ENST00000695652.1:c.2439C=	ENSP00000512083.1:p.Tyr813=
ENST00000695653.1:c.471C=	ENSP00000512084.1:p.Tyr157=
ENST00000695654.1:c.1686C=	ENSP00000512085.1:p.Tyr562=
ENST00000695655.1:c.1503C=	ENSP00000512086.1:n.1503C=
ENST00000695692.1:n.1926C=
ENST00000245907.11:c.2562C= MANE Select	ENSP00000245907.4:p.Tyr854=
ENST00000245907.10:c.2562C=	ENSP00000245907.4:p.Tyr854=
ENST00000594005.1:n.43C=
ENST00000602053.1:n.610C=
NM_000064.3:c.2562C=	NP_000055.2:p.Tyr854=
NM_000064.4:c.2562C= MANE Select	NP_000055.2:p.Tyr854=