H2AB3 H2A.B variant histone 3

Information
Symbol
H2AB3
Type
protein-coding
Description
H2A.B variant histone 3
Entrez Gene ID
83740
Genome
hg19
Position
chrX:154,689,076-154,689,666
Genome
hg38
Position
chrX:155,459,415-155,460,005
MIM
300445 OMIM
HGNC
HGNC:14455 HGNC
Ensembl
ENSG00000277745 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 H2AB2
SYNONYM H2ABBD
SYNONYM H2AFB
SYNONYM H2AFB3
MIM 300445 OMIM
HGNC HGNC:14455 HGNC
Ensembl ENSG00000277745 Ensembl
AllianceGenome HGNC:14455
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000615853.1 hg38 chrX 155,459,415 155,460,005 591
ENST00000615853.1 hg19 chrX 154,689,076 154,689,666 591
Genome browser