Canonical Allele Identifier: CA403633778

Gene: C3

Linked Data - Variant Effect Evidence

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.910C>A
ENST00000695652.1:c.2439C>A	ENSP00000512083.1:p.Tyr813Ter
ENST00000695653.1:c.471C>A	ENSP00000512084.1:p.Tyr157Ter
ENST00000695654.1:c.1686C>A	ENSP00000512085.1:p.Tyr562Ter
ENST00000695655.1:c.1503C>A	ENSP00000512086.1:n.1503C>A
ENST00000695692.1:n.1926C>A
ENST00000245907.11:c.2562C>A MANE Select	ENSP00000245907.4:p.Tyr854Ter
ENST00000245907.10:c.2562C>A	ENSP00000245907.4:p.Tyr854Ter
ENST00000594005.1:n.43C>A
ENST00000602053.1:n.610C>A
NM_000064.3:c.2562C>A	NP_000055.2:p.Tyr854Ter
NM_000064.4:c.2562C>A MANE Select	NP_000055.2:p.Tyr854Ter