Canonical Allele Identifier: CA403642309
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713296T>C , CM000681.2:g.6713296T>C GRCh38
NC_000019.9:g.6713307T>C , CM000681.1:g.6713307T>C GRCh37
NC_000019.8:g.6664307T>C NCBI36
NG_009557.1:g.12356A>G , LRG_27:g.12356A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.773A>G ENSP00000512083.1:p.Glu258Gly
ENST00000695654.1:c.20A>G ENSP00000512085.1:p.Glu7Gly
ENST00000695692.1:n.220A>G
ENST00000245907.11:c.896A>G MANE Select ENSP00000245907.4:p.Glu299Gly
ENST00000245907.10:c.896A>G ENSP00000245907.4:p.Glu299Gly
ENST00000594270.5:n.20A>G
ENST00000595577.1:n.400A>G
ENST00000597442.5:n.146A>G
NM_000064.3:c.896A>G NP_000055.2:p.Glu299Gly
NM_000064.4:c.896A>G MANE Select NP_000055.2:p.Glu299Gly