CHGB chromogranin B

Information
Symbol
CHGB
Type
protein-coding
Description
chromogranin B
Entrez Gene ID
1114
Genome
hg19
Position
chr20:5,892,156-5,905,999
Genome
hg38
Position
chr20:5,911,510-5,925,353
MIM
118920 OMIM
HGNC
HGNC:1930 HGNC
Ensembl
ENSG00000089199 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 8
Uncertain significance 0 76
Ranking
ClinVar
0
0
4
94
2
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
SYNONYM SCG1
MIM 118920 OMIM
HGNC HGNC:1930 HGNC
Ensembl ENSG00000089199 Ensembl
AllianceGenome HGNC:1930
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378961.9 hg38 chr20 5,911,510 5,925,353 13,844
ENST00000378961.9 hg19 chr20 5,892,156 5,905,999 13,844
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