C19orf47 chromosome 19 open reading frame 47

Information
Symbol
C19orf47
Type
protein-coding
Description
chromosome 19 open reading frame 47
Entrez Gene ID
126526
Genome
hg19
Position
chr19:40,825,443-40,854,434
Genome
hg38
Position
chr19:40,319,536-40,348,527
HGNC
HGNC:26723 HGNC
Ensembl
ENSG00000160392 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 3 0
Likely benign 0 2
Ranking
ClinVar
0
0
0
2
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:26723 HGNC
Ensembl ENSG00000160392 Ensembl
AllianceGenome HGNC:26723
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000683109.1 hg38 chr19 40,319,536 40,348,397 28,862
ENST00000392035.6 hg38 chr19 40,321,063 40,348,386 27,324
ENST00000582783.5 hg38 chr19 40,319,536 40,348,527 28,992
ENST00000683109.1 hg19 chr19 40,825,443 40,854,304 28,862
ENST00000582783.5 hg19 chr19 40,825,443 40,854,434 28,992
ENST00000392035.6 hg19 chr19 40,826,970 40,854,293 27,324
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