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Gene: AL590428.1 (novel transcript) Homo sapiens
Analyze
Symbol: AL590428.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101928489; uncharacterized LOC101928489
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl673,693,903 - 73,696,131 (-)EnsemblGRCh38hg38GRCh38
GRCh38673,693,903 - 73,696,131 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37674,403,959 - 74,405,743 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map6q13NCBI
HuRef671,603,464 - 71,605,247 (-)NCBIHuRef
CHM1_1674,570,048 - 74,572,274 (-)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 AL590428.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16555094
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.