ALKBH6 alkB homolog 6

Information
Symbol
ALKBH6
Type
protein-coding
Description
alkB homolog 6
Entrez Gene ID
84964
Genome
hg19
Position
chr19:36,500,107-36,505,129
Genome
hg38
Position
chr19:36,009,205-36,014,227
MIM
613304 OMIM
HGNC
HGNC:28243 HGNC
Ensembl
ENSG00000239382 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
22
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 :
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 ABH6
MIM 613304 OMIM
HGNC HGNC:28243 HGNC
Ensembl ENSG00000239382 Ensembl
AllianceGenome HGNC:28243
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000252984.11 hg38 chr19 36,009,205 36,014,227 5,023
ENST00000486389.5 hg38 chr19 36,009,124 36,014,237 5,114
ENST00000485128.5 hg38 chr19 36,009,175 36,014,239 5,065
ENST00000378875.8 hg38 chr19 36,009,120 36,014,213 5,094
ENST00000378875.8 hg19 chr19 36,500,022 36,505,115 5,094
ENST00000252984.11 hg19 chr19 36,500,107 36,505,129 5,023
ENST00000485128.5 hg19 chr19 36,500,077 36,505,141 5,065
ENST00000486389.5 hg19 chr19 36,500,026 36,505,139 5,114
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