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Gene: AC015468.1 (novel transcript) Homo sapiens
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Symbol: AC015468.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC102467222; uncharacterized LOC102467222
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl820,953,127 - 20,968,904 (+)EnsemblGRCh38hg38GRCh38
GRCh38820,953,633 - 20,968,938 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map8p21.3NCBI
CHM1_1821,013,327 - 21,028,633 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model



Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC015468.1
NCBI Gene
Ensembl Gene
JBrowse: hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16559604
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-09-08
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.