C2orf76 chromosome 2 open reading frame 76

Information
Symbol
C2orf76
Type
protein-coding
Description
chromosome 2 open reading frame 76
Entrez Gene ID
130355
Genome
hg19
Position
chr2:120,059,801-120,124,318
Genome
hg38
Position
chr2:119,302,225-119,366,742
HGNC
HGNC:27017 HGNC
Ensembl
ENSG00000186132 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 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
[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 AIM29
HGNC HGNC:27017 HGNC
Ensembl ENSG00000186132 Ensembl
AllianceGenome HGNC:27017
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000334816.12 hg38 chr2 119,302,225 119,366,834 64,610
ENST00000409877.5 hg38 chr2 119,302,444 119,366,682 64,239
ENST00000409466.6 hg38 chr2 119,302,225 119,366,742 64,518
ENST00000409523.1 hg38 chr2 119,302,444 119,366,682 64,239
ENST00000409466.6 hg19 chr2 120,059,801 120,124,318 64,518
ENST00000334816.12 hg19 chr2 120,059,801 120,124,410 64,610
ENST00000409877.5 hg19 chr2 120,060,020 120,124,258 64,239
ENST00000409523.1 hg19 chr2 120,060,020 120,124,258 64,239
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