CNN2 calponin 2

Information
Symbol
CNN2
Type
protein-coding
Description
calponin 2
Entrez Gene ID
1265
Genome
hg19
Position
chr19:1,026,628-1,039,067
Genome
hg38
Position
chr19:1,026,629-1,039,068
MIM
602373 OMIM
HGNC
HGNC:2156 HGNC
Ensembl
ENSG00000064666 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
32
4
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
MIM 602373 OMIM
HGNC HGNC:2156 HGNC
Ensembl ENSG00000064666 Ensembl
AllianceGenome HGNC:2156
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000348419.7 hg38 chr19 1,026,610 1,039,068 12,459
ENST00000568865.3 hg38 chr19 1,026,631 1,038,309 11,679
ENST00000263097.9 hg38 chr19 1,026,608 1,039,065 12,458
ENST00000562958.6 hg38 chr19 1,026,629 1,039,068 12,440
ENST00000565096.6 hg38 chr19 1,026,618 1,039,068 12,451
ENST00000263097.9 hg19 chr19 1,026,607 1,039,064 12,458
ENST00000348419.7 hg19 chr19 1,026,609 1,039,067 12,459
ENST00000565096.6 hg19 chr19 1,026,617 1,039,067 12,451
ENST00000562958.6 hg19 chr19 1,026,628 1,039,067 12,440
ENST00000568865.3 hg19 chr19 1,026,630 1,038,308 11,679
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