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Gene: AL035252.3 (novel transcript) Homo sapiens
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Symbol: AL035252.3
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: PREDICTED
Also known as: AL035252.2; LOC284798; uncharacterized LOC284798
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2025,139,652 - 25,149,372 (-)EnsemblGRCh38hg38GRCh38
GRCh382025,140,798 - 25,148,790 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372025,121,434 - 25,129,954 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map20p11.21NCBI
HuRef2025,078,749 - 25,086,741 (-)NCBIHuRef
CHM1_12025,122,338 - 25,130,330 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AL035252.3
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16554816
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.