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Gene: AC022784.1 (novel transcript) Homo sapiens
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Symbol: AC022784.1
Name: novel transcript
CRRD ID: 16558181
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101929128; LOC157273; uncharacterized LOC101929128; uncharacterized LOC157273
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl89,151,695 - 9,425,524 (+)EnsemblGRCh38hg38GRCh38
GRCh3889,325,051 - 9,335,080 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3789,182,561 - 9,192,590 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.1NCBI
HuRef88,108,763 - 8,118,798 (+)NCBIHuRef
CHM1_189,247,880 - 9,257,909 (+)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 AC022784.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16558181
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.