Canonical Allele Identifier: CA403633983
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs761759483

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697726A>T , CM000681.2:g.6697726A>T GRCh38
NC_000019.9:g.6697737A>T , CM000681.1:g.6697737A>T GRCh37
NC_000019.8:g.6648737A>T NCBI36
NG_009557.1:g.27926T>A , LRG_27:g.27926T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.857T>A
ENST00000695652.1:c.2386T>A ENSP00000512083.1:p.Tyr796Asn
ENST00000695653.1:c.418T>A ENSP00000512084.1:p.Tyr140Asn
ENST00000695654.1:c.1633T>A ENSP00000512085.1:p.Tyr545Asn
ENST00000695655.1:c.1450T>A ENSP00000512086.1:n.1450T>A
ENST00000695692.1:n.1873T>A
ENST00000245907.11:c.2509T>A MANE Select ENSP00000245907.4:p.Tyr837Asn
ENST00000245907.10:c.2509T>A ENSP00000245907.4:p.Tyr837Asn
ENST00000602053.1:n.557T>A
NM_000064.3:c.2509T>A NP_000055.2:p.Tyr837Asn
NM_000064.4:c.2509T>A MANE Select NP_000055.2:p.Tyr837Asn