H2AB2 H2A.B variant histone 2

Information
Symbol
H2AB2
Type
protein-coding
Description
H2A.B variant histone 2
Entrez Gene ID
474381
Genome
hg19
Position
chrX:154,610,358-154,610,948
Genome
hg38
Position
chrX:155,380,709-155,381,299
MIM
301038 OMIM
HGNC
HGNC:18298 HGNC
Ensembl
ENSG00000277858 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
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 H2A.B.1
SYNONYM H2A.Bbd
SYNONYM H2AB3
SYNONYM H2AFB2
MIM 301038 OMIM
HGNC HGNC:18298 HGNC
Ensembl ENSG00000277858 Ensembl
AllianceGenome HGNC:18298
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000354514.6 hg38 chrX 155,380,709 155,381,299 591
ENST00000354514.6 hg19 chrX 154,610,358 154,610,948 591
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