Canonical Allele Identifier: CA559800367
Gene: CDC20B HGNC NCBI
MIR449B HGNC NCBI

Linked Data

dbSNP Id: rs1358529452

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55170677_55170681del , CM000667.2:g.55170677_55170681del GRCh38
NC_000005.9:g.54466505_54466509del , CM000667.1:g.54466505_54466509del GRCh37
NC_000005.8:g.54502262_54502266del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381375.7:c.126+1907_126+1911del (CDC20B) MANE Select ENSP00000370781.2:n.126+1907_126+1911del
ENST00000296733.5:c.126+1907_126+1911del (CDC20B) ENSP00000296733.1:n.126+1907_126+1911del
ENST00000322374.10:c.126+1907_126+1911del (CDC20B) ENSP00000315720.6:n.126+1907_126+1911del
ENST00000381375.6:c.126+1907_126+1911del (CDC20B) ENSP00000370781.2:n.126+1907_126+1911del
ENST00000507931.1:c.63+2257_63+2261del (CDC20B) ENSP00000423919.1:n.63+2257_63+2261del
ENST00000513180.5:c.126+1907_126+1911del (CDC20B) ENSP00000426776.1:n.126+1907_126+1911del
NM_001145734.2:c.126+1907_126+1911del (CDC20B) NP_001139206.2:n.126+1907_126+1911del
NM_001170402.1:c.126+1907_126+1911del (CDC20B) MANE Select NP_001163873.1:n.126+1907_126+1911del
NM_152623.2:c.126+1907_126+1911del (CDC20B) NP_689836.2:n.126+1907_126+1911del
NR_030387.1:n.62_66del (MIR449B)
XM_011543218.1:c.126+1907_126+1911del (CDC20B) XP_011541520.1:n.126+1907_126+1911del
XM_011543218.2:c.126+1907_126+1911del (CDC20B) XP_011541520.1:n.126+1907_126+1911del