HMG20B high mobility group 20B

Information
Symbol
HMG20B
Type
protein-coding
Description
high mobility group 20B
Entrez Gene ID
10362
Genome
hg19
Position
chr19:3,572,942-3,579,081
Genome
hg38
Position
chr19:3,572,944-3,579,083
MIM
605535 OMIM
HGNC
HGNC:5002 HGNC
Ensembl
ENSG00000064961 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
24
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
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Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM BRAF25
SYNONYM BRAF35
SYNONYM HMGX2
SYNONYM HMGXB2
SYNONYM PP7706
SYNONYM SMARCE1r
SYNONYM SOXL
SYNONYM pp8857
MIM 605535 OMIM
HGNC HGNC:5002 HGNC
Ensembl ENSG00000064961 Ensembl
AllianceGenome HGNC:5002
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000333651.11 hg38 chr19 3,572,944 3,579,083 6,140
ENST00000333651.11 hg19 chr19 3,572,942 3,579,081 6,140
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