Canonical Allele Identifier: CA403640714
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710838T>A , CM000681.2:g.6710838T>A GRCh38
NC_000019.9:g.6710849T>A , CM000681.1:g.6710849T>A GRCh37
NC_000019.8:g.6661849T>A NCBI36
NG_009557.1:g.14814A>T , LRG_27:g.14814A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1364A>T ENSP00000512083.1:p.Asn455Ile
ENST00000695654.1:c.611A>T ENSP00000512085.1:p.Asn204Ile
ENST00000695655.1:c.392A>T ENSP00000512086.1:p.Asn131Ile
ENST00000695692.1:n.851A>T
ENST00000245907.11:c.1487A>T MANE Select ENSP00000245907.4:p.Asn496Ile
ENST00000245907.10:c.1487A>T ENSP00000245907.4:p.Asn496Ile
ENST00000600763.1:n.120A>T
NM_000064.3:c.1487A>T NP_000055.2:p.Asn496Ile
NM_000064.4:c.1487A>T MANE Select NP_000055.2:p.Asn496Ile