CHRNG cholinergic receptor nicotinic gamma subunit

Information
Symbol
CHRNG
Type
protein-coding
Description
cholinergic receptor nicotinic gamma subunit
Entrez Gene ID
1146
Genome
hg19
Position
chr2:233,404,402-233,412,825
Genome
hg38
Position
chr2:232,539,692-232,548,115
MIM
100730 OMIM
HGNC
HGNC:1967 HGNC
Ensembl
ENSG00000196811 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 80
Likely pathogenic 0 42
Benign 0 70
Likely benign 0 524
Conflicting classifications of pathogenicity 0 78
Uncertain significance 0 174
Ranking
ClinVar
0
0
86
776
6
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 :
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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 ACHRG
MIM 100730 OMIM
HGNC HGNC:1967 HGNC
Ensembl ENSG00000196811 Ensembl
AllianceGenome HGNC:1967
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000389492.3 hg38 chr2 232,539,748 232,545,716 5,969
ENST00000651502.1 hg38 chr2 232,539,692 232,548,115 8,424
ENST00000651502.1 hg19 chr2 233,404,402 233,412,825 8,424
ENST00000389492.3 hg19 chr2 233,404,458 233,410,426 5,969
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