Canonical Allele Identifier: CA403642100
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713217G>C , CM000681.2:g.6713217G>C GRCh38
NC_000019.9:g.6713228G>C , CM000681.1:g.6713228G>C GRCh37
NC_000019.8:g.6664228G>C NCBI36
NG_009557.1:g.12435C>G , LRG_27:g.12435C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.852C>G ENSP00000512083.1:p.Tyr284Ter
ENST00000695654.1:c.99C>G ENSP00000512085.1:p.Tyr33Ter
ENST00000695692.1:n.299C>G
ENST00000245907.11:c.975C>G MANE Select ENSP00000245907.4:p.Tyr325Ter
ENST00000245907.10:c.975C>G ENSP00000245907.4:p.Tyr325Ter
ENST00000594270.5:n.99C>G
ENST00000595577.1:n.479C>G
ENST00000597442.5:n.225C>G
NM_000064.3:c.975C>G NP_000055.2:p.Tyr325Ter
NM_000064.4:c.975C>G MANE Select NP_000055.2:p.Tyr325Ter