IGHV4-39 immunoglobulin heavy variable 4-39

Information
Symbol
IGHV4-39
Type
other
Description
immunoglobulin heavy variable 4-39
Entrez Gene ID
28394
Genome
hg19
Position
chr14:106,877,619-106,878,126
Genome
hg38
Position
chr14:106,421,711-106,422,218
HGNC
HGNC:5651 HGNC
Ensembl
ENSG00000211959 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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 IGHV439
SYNONYM VH
HGNC HGNC:5651 HGNC
Ensembl ENSG00000211959 Ensembl
IMGT/GENE-DB IGHV4-39
AllianceGenome HGNC:5651
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000390619.2 hg38 chr14 106,421,711 106,422,218 508
ENST00000390619.2 hg19 chr14 106,877,619 106,878,126 508
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