Canonical Allele Identifier: CA3266457
Gene: CDC20B HGNC NCBI
MIR449B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10061133

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55170716A>G , CM000667.2:g.55170716A>G GRCh38
NC_000005.9:g.54466544A>G , CM000667.1:g.54466544A>G GRCh37
NC_000005.8:g.54502301A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001145734.2:c.126+1872T>C (CDC20B) VV NP_001139206.2:p.=
NM_001170402.1:c.126+1872T>C (CDC20B) VV NP_001163873.1:p.=
NM_152623.2:c.126+1872T>C (CDC20B) VV NP_689836.2:p.=
NR_030387.1:n.27T>C (MIR449B)
XM_011543218.1:c.126+1872T>C (CDC20B) XP_011541520.1:p.=
XM_011543218.2:c.126+1872T>C (CDC20B)
ENST00000296733.5:c.126+1872T>C ENSP00000296733.1:p.=
ENST00000322374.10:c.126+1872T>C ENSP00000315720.6:p.=
ENST00000381375.6:c.126+1872T>C ENSP00000370781.2:p.=
ENST00000507931.1:c.63+2222T>C ENSP00000423919.1:p.=
ENST00000513180.5:c.126+1872T>C ENSP00000426776.1:p.=