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Gene: AF131215.3 (novel transcript) Homo sapiens
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Symbol: AF131215.3
Name: novel transcript
CRRD ID: 16560455
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101929269; uncharacterized LOC101929269
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl811,062,647 - 11,067,089 (-)EnsemblGRCh38hg38GRCh38
GRCh38811,062,652 - 11,067,089 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37810,920,162 - 10,924,599 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.1NCBI
HuRef89,850,378 - 9,854,815 (-)NCBIHuRef
CHM1_1810,985,406 - 10,989,848 (-)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 AF131215.3
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16560455
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-09-16
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.