Canonical Allele Identifier: CA403642189
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713258G>C , CM000681.2:g.6713258G>C GRCh38
NC_000019.9:g.6713269G>C , CM000681.1:g.6713269G>C GRCh37
NC_000019.8:g.6664269G>C NCBI36
NG_009557.1:g.12394C>G , LRG_27:g.12394C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.811C>G ENSP00000512083.1:p.Gln271Glu
ENST00000695654.1:c.58C>G ENSP00000512085.1:p.Gln20Glu
ENST00000695692.1:n.258C>G
ENST00000245907.11:c.934C>G MANE Select ENSP00000245907.4:p.Gln312Glu
ENST00000245907.10:c.934C>G ENSP00000245907.4:p.Gln312Glu
ENST00000594270.5:n.58C>G
ENST00000595577.1:n.438C>G
ENST00000597442.5:n.184C>G
NM_000064.3:c.934C>G NP_000055.2:p.Gln312Glu
NM_000064.4:c.934C>G MANE Select NP_000055.2:p.Gln312Glu