Canonical Allele Identifier: CA2320559195
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697724G= , CM000681.2:g.6697724G= GRCh38
NC_000019.9:g.6697735G= , CM000681.1:g.6697735G= GRCh37
NC_000019.8:g.6648735G= NCBI36
NG_009557.1:g.27928C= , LRG_27:g.27928C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.859C=
ENST00000695652.1:c.2388C= ENSP00000512083.1:p.Tyr796=
ENST00000695653.1:c.420C= ENSP00000512084.1:p.Tyr140=
ENST00000695654.1:c.1635C= ENSP00000512085.1:p.Tyr545=
ENST00000695655.1:c.1452C= ENSP00000512086.1:n.1452C=
ENST00000695692.1:n.1875C=
ENST00000245907.11:c.2511C= MANE Select ENSP00000245907.4:p.Tyr837=
ENST00000245907.10:c.2511C= ENSP00000245907.4:p.Tyr837=
ENST00000602053.1:n.559C=
NM_000064.3:c.2511C= NP_000055.2:p.Tyr837=
NM_000064.4:c.2511C= MANE Select NP_000055.2:p.Tyr837=