H2BW2 H2B.W histone 2

Information
Symbol
H2BW2
Type
protein-coding
Description
H2B.W histone 2
Entrez Gene ID
286436
Genome
hg19
Position
chrX:103,294,523-103,297,021
Genome
hg38
Position
chrX:104,039,956-104,042,454
HGNC
HGNC:27867 HGNC
Ensembl
ENSG00000101812 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
44
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 H2B/s
SYNONYM H2BFM
SYNONYM H2BM
HGNC HGNC:27867 HGNC
Ensembl ENSG00000101812 Ensembl
AllianceGenome HGNC:27867
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000675318.3 hg38 chrX 104,039,956 104,042,454 2,499
ENST00000355016.8 hg38 chrX 104,039,956 104,042,454 2,499
ENST00000355016.8 hg19 chrX 103,294,523 103,297,021 2,499
ENST00000675318.3 hg19 chrX 103,294,523 103,297,021 2,499
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