Canonical Allele Identifier: CA2320559193
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697718A= , CM000681.2:g.6697718A= GRCh38
NC_000019.9:g.6697729A= , CM000681.1:g.6697729A= GRCh37
NC_000019.8:g.6648729A= NCBI36
NG_009557.1:g.27934T= , LRG_27:g.27934T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.865T=
ENST00000695652.1:c.2394T= ENSP00000512083.1:p.Val798=
ENST00000695653.1:c.426T= ENSP00000512084.1:p.Val142=
ENST00000695654.1:c.1641T= ENSP00000512085.1:p.Val547=
ENST00000695655.1:c.1458T= ENSP00000512086.1:n.1458T=
ENST00000695692.1:n.1881T=
ENST00000245907.11:c.2517T= MANE Select ENSP00000245907.4:p.Val839=
ENST00000245907.10:c.2517T= ENSP00000245907.4:p.Val839=
ENST00000602053.1:n.565T=
NM_000064.3:c.2517T= NP_000055.2:p.Val839=
NM_000064.4:c.2517T= MANE Select NP_000055.2:p.Val839=