NFYB nuclear transcription factor Y subunit beta

Information
Symbol
NFYB
Type
protein-coding
Description
nuclear transcription factor Y subunit beta
Entrez Gene ID
4801
Genome
hg19
Position
chr12:104,510,864-104,531,988
Genome
hg38
Position
chr12:104,117,086-104,138,210
MIM
189904 OMIM
HGNC
HGNC:7805 HGNC
Ensembl
ENSG00000120837 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
10
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 CBF-A
SYNONYM CBF-B
SYNONYM HAP3
SYNONYM NF-YB
MIM 189904 OMIM
HGNC HGNC:7805 HGNC
Ensembl ENSG00000120837 Ensembl
AllianceGenome HGNC:7805
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000551446.6 hg38 chr12 104,117,118 104,138,241 21,124
ENST00000551727.5 hg38 chr12 104,119,355 104,138,017 18,663
ENST00000240055.8 hg38 chr12 104,117,086 104,138,210 21,125
ENST00000240055.8 hg19 chr12 104,510,864 104,531,988 21,125
ENST00000551446.6 hg19 chr12 104,510,896 104,532,019 21,124
ENST00000551727.5 hg19 chr12 104,513,133 104,531,795 18,663
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