ENST00000667851.1 NHIP

Information
Transcript ID
ENST00000667851.1
Genome
hg19
Position
chr22:49,443,303-49,448,361
Strand
-
CDS length
0
Amino acid length
0
Gene symbol
NHIP
Gene type
ncRNA
Gene description
neuronal hypoxia inducible, placenta associated
Gene Entrez Gene ID
105373085
Variants

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Target data :
MGeND data only
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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
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MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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Target data :
MGeND data only
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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
Exon
Exon number Start Stop
3 49,443,303 49,444,761
2 49,445,207 49,445,358
1 49,446,168 49,448,361
Other genome
Genome Chromosome Start End Links
hg38 chr22 49,047,491 49,052,549 Link
CDS sequence
Amino sequence