Canonical Allele Identifier: CA444181139

Gene: CDC20B MIR449B

Linked Data

• dbSNP Id: rs1400482017
• gnomAD v2: 5-54466567-G-A
• gnomAD v4: 5-55170739-G-A
• MyVariant Identifiers: chr5:g.54466567G>A (hg19) ; chr5:g.55170739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55170739G>A , CM000667.2:g.55170739G>A	GRCh38
NC_000005.9:g.54466567G>A , CM000667.1:g.54466567G>A	GRCh37
NC_000005.8:g.54502324G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381375.7:c.126+1849C>T (CDC20B) MANE Select	ENSP00000370781.2:n.126+1849C>T
ENST00000296733.5:c.126+1849C>T (CDC20B)	ENSP00000296733.1:n.126+1849C>T
ENST00000322374.10:c.126+1849C>T (CDC20B)	ENSP00000315720.6:n.126+1849C>T
ENST00000381375.6:c.126+1849C>T (CDC20B)	ENSP00000370781.2:n.126+1849C>T
ENST00000507931.1:c.63+2199C>T (CDC20B)	ENSP00000423919.1:n.63+2199C>T
ENST00000513180.5:c.126+1849C>T (CDC20B)	ENSP00000426776.1:n.126+1849C>T
NM_001145734.2:c.126+1849C>T (CDC20B)	NP_001139206.2:n.126+1849C>T
NM_001170402.1:c.126+1849C>T (CDC20B) MANE Select	NP_001163873.1:n.126+1849C>T
NM_152623.2:c.126+1849C>T (CDC20B)	NP_689836.2:n.126+1849C>T
NR_030387.1:n.4C>T (MIR449B)
XM_011543218.1:c.126+1849C>T (CDC20B)	XP_011541520.1:n.126+1849C>T
XM_011543218.2:c.126+1849C>T (CDC20B)	XP_011541520.1:n.126+1849C>T