Canonical Allele Identifier: CA403643127
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714180T>G , CM000681.2:g.6714180T>G GRCh38
NC_000019.9:g.6714191T>G , CM000681.1:g.6714191T>G GRCh37
NC_000019.8:g.6665191T>G NCBI36
NG_009557.1:g.11472A>C , LRG_27:g.11472A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.545A>C ENSP00000512083.1:p.Glu182Ala
ENST00000245907.11:c.668A>C MANE Select ENSP00000245907.4:p.Glu223Ala
ENST00000245907.10:c.668A>C ENSP00000245907.4:p.Glu223Ala
ENST00000595577.1:n.172A>C
NM_000064.3:c.668A>C NP_000055.2:p.Glu223Ala
NM_000064.4:c.668A>C MANE Select NP_000055.2:p.Glu223Ala