Canonical Allele Identifier: CA403642129
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713230C>T , CM000681.2:g.6713230C>T GRCh38
NC_000019.9:g.6713241C>T , CM000681.1:g.6713241C>T GRCh37
NC_000019.8:g.6664241C>T NCBI36
NG_009557.1:g.12422G>A , LRG_27:g.12422G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.839G>A ENSP00000512083.1:p.Gly280Glu
ENST00000695654.1:c.86G>A ENSP00000512085.1:p.Gly29Glu
ENST00000695692.1:n.286G>A
ENST00000245907.11:c.962G>A MANE Select ENSP00000245907.4:p.Gly321Glu
ENST00000245907.10:c.962G>A ENSP00000245907.4:p.Gly321Glu
ENST00000594270.5:n.86G>A
ENST00000595577.1:n.466G>A
ENST00000597442.5:n.212G>A
NM_000064.3:c.962G>A NP_000055.2:p.Gly321Glu
NM_000064.4:c.962G>A MANE Select NP_000055.2:p.Gly321Glu