SEC61G-DT SEC61G divergent transcript

Information
Symbol
SEC61G-DT
Type
ncRNA
Description
SEC61G divergent transcript
Entrez Gene ID
100996654
Genome
hg19
Position
chr7:54,827,041-54,880,420
Genome
hg38
Position
chr7:54,759,348-54,812,727
HGNC
HGNC:40835 HGNC
Ensembl
ENSG00000234707 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 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
HGNC HGNC:40835 HGNC
Ensembl ENSG00000234707 Ensembl
AllianceGenome HGNC:40835
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000691743.1 hg38 chr7 54,759,328 54,804,969 45,642
ENST00000655633.1 hg38 chr7 54,759,348 54,812,727 53,380
ENST00000691743.1 hg19 chr7 54,827,021 54,872,662 45,642
ENST00000655633.1 hg19 chr7 54,827,041 54,880,420 53,380
Genome browser