Canonical Allele Identifier: CA403643219
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714220A>T , CM000681.2:g.6714220A>T GRCh38
NC_000019.9:g.6714231A>T , CM000681.1:g.6714231A>T GRCh37
NC_000019.8:g.6665231A>T NCBI36
NG_009557.1:g.11432T>A , LRG_27:g.11432T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.505T>A ENSP00000512083.1:p.Tyr169Asn
ENST00000245907.11:c.628T>A MANE Select ENSP00000245907.4:p.Tyr210Asn
ENST00000245907.10:c.628T>A ENSP00000245907.4:p.Tyr210Asn
ENST00000595577.1:n.132T>A
NM_000064.3:c.628T>A NP_000055.2:p.Tyr210Asn
NM_000064.4:c.628T>A MANE Select NP_000055.2:p.Tyr210Asn