Canonical Allele Identifier: CA403639521
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709802A>T , CM000681.2:g.6709802A>T GRCh38
NC_000019.9:g.6709813A>T , CM000681.1:g.6709813A>T GRCh37
NC_000019.8:g.6660813A>T NCBI36
NG_009557.1:g.15850T>A , LRG_27:g.15850T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1604T>A ENSP00000512083.1:p.Val535Glu
ENST00000695654.1:c.851T>A ENSP00000512085.1:p.Val284Glu
ENST00000695655.1:c.668T>A ENSP00000512086.1:n.668T>A
ENST00000695692.1:n.1091T>A
ENST00000245907.11:c.1727T>A MANE Select ENSP00000245907.4:p.Val576Glu
ENST00000245907.10:c.1727T>A ENSP00000245907.4:p.Val576Glu
ENST00000600763.1:n.360T>A
NM_000064.3:c.1727T>A NP_000055.2:p.Val576Glu
NM_000064.4:c.1727T>A MANE Select NP_000055.2:p.Val576Glu