Canonical Allele Identifier: CA403642176
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713253G>T , CM000681.2:g.6713253G>T GRCh38
NC_000019.9:g.6713264G>T , CM000681.1:g.6713264G>T GRCh37
NC_000019.8:g.6664264G>T NCBI36
NG_009557.1:g.12399C>A , LRG_27:g.12399C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.816C>A ENSP00000512083.1:p.Asn272Lys
ENST00000695654.1:c.63C>A ENSP00000512085.1:p.Asn21Lys
ENST00000695692.1:n.263C>A
ENST00000245907.11:c.939C>A MANE Select ENSP00000245907.4:p.Asn313Lys
ENST00000245907.10:c.939C>A ENSP00000245907.4:p.Asn313Lys
ENST00000594270.5:n.63C>A
ENST00000595577.1:n.443C>A
ENST00000597442.5:n.189C>A
NM_000064.3:c.939C>A NP_000055.2:p.Asn313Lys
NM_000064.4:c.939C>A MANE Select NP_000055.2:p.Asn313Lys