ENST00000401279.1 MIR892B

Information
Transcript ID
ENST00000401279.1
Genome
hg38
Position
chrX:145,997,198-145,997,274
Strand
-
CDS length
0
Amino acid length
0
Gene symbol
MIR892B
Gene type
ncRNA
Gene description
microRNA 892b
Gene Entrez Gene ID
100126307
Variants

Display target variant


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
Exon
Exon number Start Stop
1 145,997,198 145,997,274
Other genome
Genome Chromosome Start End Links
hg19 chrX 145,078,716 145,078,792 Link
CDS sequence
Amino sequence