Canonical Allele Identifier: CA2320570613
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6718290G= , CM000681.2:g.6718290G= GRCh38
NC_000019.9:g.6718301G= , CM000681.1:g.6718301G= GRCh37
NC_000019.8:g.6669301G= NCBI36
NG_009557.1:g.7362C= , LRG_27:g.7362C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000594936.2:n.451C=
ENST00000695652.1:c.267C= ENSP00000512083.1:p.Leu89=
ENST00000695693.1:c.390C= ENSP00000512104.1:p.Leu130=
ENST00000245907.11:c.390C= MANE Select ENSP00000245907.4:p.Leu130=
ENST00000245907.10:c.390C= ENSP00000245907.4:p.Leu130=
ENST00000594936.1:n.451C=
ENST00000600744.1:c.267C= ENSP00000472044.1:p.Leu89=
NM_000064.3:c.390C= NP_000055.2:p.Leu130=
NM_000064.4:c.390C= MANE Select NP_000055.2:p.Leu130=