Canonical Allele Identifier: CA403642655
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713465A>T , CM000681.2:g.6713465A>T GRCh38
NC_000019.9:g.6713476A>T , CM000681.1:g.6713476A>T GRCh37
NC_000019.8:g.6664476A>T NCBI36
NG_009557.1:g.12187T>A , LRG_27:g.12187T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.695T>A ENSP00000512083.1:p.Phe232Tyr
ENST00000695692.1:n.142T>A
ENST00000245907.11:c.818T>A MANE Select ENSP00000245907.4:p.Phe273Tyr
ENST00000245907.10:c.818T>A ENSP00000245907.4:p.Phe273Tyr
ENST00000595577.1:n.322T>A
ENST00000597442.5:n.68T>A
NM_000064.3:c.818T>A NP_000055.2:p.Phe273Tyr
NM_000064.4:c.818T>A MANE Select NP_000055.2:p.Phe273Tyr