Canonical Allele Identifier: CA403639319
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709739G>C , CM000681.2:g.6709739G>C GRCh38
NC_000019.9:g.6709750G>C , CM000681.1:g.6709750G>C GRCh37
NC_000019.8:g.6660750G>C NCBI36
NG_009557.1:g.15913C>G , LRG_27:g.15913C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1667C>G ENSP00000512083.1:p.Ala556Gly
ENST00000695654.1:c.914C>G ENSP00000512085.1:p.Ala305Gly
ENST00000695655.1:c.731C>G ENSP00000512086.1:n.731C>G
ENST00000695692.1:n.1154C>G
ENST00000245907.11:c.1790C>G MANE Select ENSP00000245907.4:p.Ala597Gly
ENST00000245907.10:c.1790C>G ENSP00000245907.4:p.Ala597Gly
NM_000064.3:c.1790C>G NP_000055.2:p.Ala597Gly
NM_000064.4:c.1790C>G MANE Select NP_000055.2:p.Ala597Gly