Canonical Allele Identifier: CA403640709
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1458826211
gnomAD v2: 19-6710848-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710837G>T , CM000681.2:g.6710837G>T GRCh38
NC_000019.9:g.6710848G>T , CM000681.1:g.6710848G>T GRCh37
NC_000019.8:g.6661848G>T NCBI36
NG_009557.1:g.14815C>A , LRG_27:g.14815C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1365C>A ENSP00000512083.1:p.Asn455Lys
ENST00000695654.1:c.612C>A ENSP00000512085.1:p.Asn204Lys
ENST00000695655.1:c.393C>A ENSP00000512086.1:p.Asn131Lys
ENST00000695692.1:n.852C>A
ENST00000245907.11:c.1488C>A MANE Select ENSP00000245907.4:p.Asn496Lys
ENST00000245907.10:c.1488C>A ENSP00000245907.4:p.Asn496Lys
ENST00000600763.1:n.121C>A
NM_000064.3:c.1488C>A NP_000055.2:p.Asn496Lys
NM_000064.4:c.1488C>A MANE Select NP_000055.2:p.Asn496Lys