Canonical Allele Identifier: CA1547364605

Gene: CDC20B MIR449B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55170647G= , CM000667.2:g.55170647G=	GRCh38
NC_000005.9:g.54466475G= , CM000667.1:g.54466475G=	GRCh37
NC_000005.8:g.54502232G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381375.7:c.126+1941C= (CDC20B) MANE Select	ENSP00000370781.2:n.126+1941C=
ENST00000296733.5:c.126+1941C= (CDC20B)	ENSP00000296733.1:n.126+1941C=
ENST00000322374.10:c.126+1941C= (CDC20B)	ENSP00000315720.6:n.126+1941C=
ENST00000381375.6:c.126+1941C= (CDC20B)	ENSP00000370781.2:n.126+1941C=
ENST00000507931.1:c.63+2291C= (CDC20B)	ENSP00000423919.1:n.63+2291C=
ENST00000513180.5:c.126+1941C= (CDC20B)	ENSP00000426776.1:n.126+1941C=
NM_001145734.2:c.126+1941C= (CDC20B)	NP_001139206.2:n.126+1941C=
NM_001170402.1:c.126+1941C= (CDC20B) MANE Select	NP_001163873.1:n.126+1941C=
NM_152623.2:c.126+1941C= (CDC20B)	NP_689836.2:n.126+1941C=
NR_030387.1:n.96C= (MIR449B)
XM_011543218.1:c.126+1941C= (CDC20B)	XP_011541520.1:n.126+1941C=
XM_011543218.2:c.126+1941C= (CDC20B)	XP_011541520.1:n.126+1941C=