GOLGA8H golgin A8 family member H

Information
Symbol
GOLGA8H
Type
protein-coding
Description
golgin A8 family member H
Entrez Gene ID
728498
Genome
hg19
Position
chr15:30,896,231-30,909,955
Genome
hg38
Position
chr15:30,604,028-30,617,752
HGNC
HGNC:37443 HGNC
Ensembl
ENSG00000261794 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 5 0
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
SYNONYM GOLGA6L11
HGNC HGNC:37443 HGNC
Ensembl ENSG00000261794 Ensembl
AllianceGenome HGNC:37443
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000566740.2 hg38 chr15 30,604,028 30,617,752 13,725
ENST00000566740.2 hg19 chr15 30,896,231 30,909,955 13,725
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