CHFR-DT CHFR divergent transcript

Information
Symbol
CHFR-DT
Type
ncRNA
Description
CHFR divergent transcript
Entrez Gene ID
101928530
Genome
hg19
Position
chr12:133,464,428-133,465,169
Genome
hg38
Position
chr12:132,887,842-132,888,583
HGNC
HGNC:55658 HGNC
Ensembl
ENSG00000236617 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[No Data.]
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
HGNC HGNC:55658 HGNC
Ensembl ENSG00000236617 Ensembl
AllianceGenome HGNC:55658
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000424075.2 hg38 chr12 132,887,842 132,888,583 742
ENST00000424075.2 hg19 chr12 133,464,428 133,465,169 742
Genome browser