Canonical Allele Identifier: CA403642319
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713299C>A , CM000681.2:g.6713299C>A GRCh38
NC_000019.9:g.6713310C>A , CM000681.1:g.6713310C>A GRCh37
NC_000019.8:g.6664310C>A NCBI36
NG_009557.1:g.12353G>T , LRG_27:g.12353G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.770G>T ENSP00000512083.1:p.Gly257Val
ENST00000695654.1:c.17G>T ENSP00000512085.1:p.Gly6Val
ENST00000695692.1:n.217G>T
ENST00000245907.11:c.893G>T MANE Select ENSP00000245907.4:p.Gly298Val
ENST00000245907.10:c.893G>T ENSP00000245907.4:p.Gly298Val
ENST00000594270.5:n.17G>T
ENST00000595577.1:n.397G>T
ENST00000597442.5:n.143G>T
NM_000064.3:c.893G>T NP_000055.2:p.Gly298Val
NM_000064.4:c.893G>T MANE Select NP_000055.2:p.Gly298Val