HMGB3 high mobility group box 3

Information
Symbol
HMGB3
Type
protein-coding
Description
high mobility group box 3
Entrez Gene ID
3149
Genome
hg19
Position
chrX:150,151,808-150,159,244
Genome
hg38
Position
chrX:150,983,335-150,990,771
MIM
300193 OMIM
HGNC
HGNC:5004 HGNC
Ensembl
ENSG00000029993 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
not provided 6 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
2
14
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 :
Filtering :
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 HMG-2a
SYNONYM HMG-4
SYNONYM HMG2A
SYNONYM HMG4
MIM 300193 OMIM
HGNC HGNC:5004 HGNC
Ensembl ENSG00000029993 Ensembl
AllianceGenome HGNC:5004
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000325307.12 hg38 chrX 150,983,335 150,990,771 7,437
ENST00000448905.6 hg38 chrX 150,983,406 150,987,932 4,527
ENST00000325307.12 hg19 chrX 150,151,808 150,159,244 7,437
ENST00000448905.6 hg19 chrX 150,151,879 150,156,405 4,527
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