Canonical Allele Identifier: CA9129742
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs746042506
gnomAD v2: 19-6714226-T-C
gnomAD v3: 19-6714215-T-C
gnomAD v4: 19-6714215-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714215T>C , CM000681.2:g.6714215T>C GRCh38
NC_000019.9:g.6714226T>C , CM000681.1:g.6714226T>C GRCh37
NC_000019.8:g.6665226T>C NCBI36
NG_009557.1:g.11437A>G , LRG_27:g.11437A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.510A>G ENSP00000512083.1:p.Glu170=
ENST00000245907.11:c.633A>G MANE Select ENSP00000245907.4:p.Glu211=
ENST00000245907.10:c.633A>G ENSP00000245907.4:p.Glu211=
ENST00000595577.1:n.137A>G
NM_000064.3:c.633A>G NP_000055.2:p.Glu211=
NM_000064.4:c.633A>G MANE Select NP_000055.2:p.Glu211=