Canonical Allele Identifier: CA118946318

Gene: CDC20B MIR449B

Linked Data

• dbSNP Id: rs1045697233
• MyVariant Identifiers: chr5:g.54466556A>G (hg19) ; chr5:g.55170728A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55170728A>G , CM000667.2:g.55170728A>G	GRCh38
NC_000005.9:g.54466556A>G , CM000667.1:g.54466556A>G	GRCh37
NC_000005.8:g.54502313A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381375.7:c.126+1860T>C (CDC20B) MANE Select	ENSP00000370781.2:n.126+1860T>C
ENST00000296733.5:c.126+1860T>C (CDC20B)	ENSP00000296733.1:n.126+1860T>C
ENST00000322374.10:c.126+1860T>C (CDC20B)	ENSP00000315720.6:n.126+1860T>C
ENST00000381375.6:c.126+1860T>C (CDC20B)	ENSP00000370781.2:n.126+1860T>C
ENST00000507931.1:c.63+2210T>C (CDC20B)	ENSP00000423919.1:n.63+2210T>C
ENST00000513180.5:c.126+1860T>C (CDC20B)	ENSP00000426776.1:n.126+1860T>C
NM_001145734.2:c.126+1860T>C (CDC20B)	NP_001139206.2:n.126+1860T>C
NM_001170402.1:c.126+1860T>C (CDC20B) MANE Select	NP_001163873.1:n.126+1860T>C
NM_152623.2:c.126+1860T>C (CDC20B)	NP_689836.2:n.126+1860T>C
NR_030387.1:n.15T>C (MIR449B)
XM_011543218.1:c.126+1860T>C (CDC20B)	XP_011541520.1:n.126+1860T>C
XM_011543218.2:c.126+1860T>C (CDC20B)	XP_011541520.1:n.126+1860T>C