Canonical Allele Identifier: CA403639552
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709811C>G , CM000681.2:g.6709811C>G GRCh38
NC_000019.9:g.6709822C>G , CM000681.1:g.6709822C>G GRCh37
NC_000019.8:g.6660822C>G NCBI36
NG_009557.1:g.15841G>C , LRG_27:g.15841G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1595G>C ENSP00000512083.1:p.Arg532Pro
ENST00000695654.1:c.842G>C ENSP00000512085.1:p.Arg281Pro
ENST00000695655.1:c.659G>C ENSP00000512086.1:n.659G>C
ENST00000695692.1:n.1082G>C
ENST00000245907.11:c.1718G>C MANE Select ENSP00000245907.4:p.Arg573Pro
ENST00000245907.10:c.1718G>C ENSP00000245907.4:p.Arg573Pro
ENST00000600763.1:n.351G>C
NM_000064.3:c.1718G>C NP_000055.2:p.Arg573Pro
NM_000064.4:c.1718G>C MANE Select NP_000055.2:p.Arg573Pro