ENST00000667851.1 NHIP

Information
Transcript ID
ENST00000667851.1
Genome
hg38
Position
chr22:49,047,491-49,052,549
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

Display target variant


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
Exon
Exon number Start Stop
3 49,047,491 49,048,949
2 49,049,395 49,049,546
1 49,050,356 49,052,549
Other genome
Genome Chromosome Start End Links
hg19 chr22 49,443,303 49,448,361 Link
CDS sequence
Amino sequence