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Gene: AC107959.4 (novel transcript) Homo sapiens
Analyze
Symbol: AC107959.4
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC254896; uncharacterized LOC254896
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl823,084,355 - 23,103,558 (+)EnsemblGRCh38hg38GRCh38
GRCh38823,084,355 - 23,103,558 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37822,941,868 - 22,961,071 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p21.3NCBI
HuRef821,486,016 - 21,505,218 (+)NCBIHuRef
CHM1_1823,143,936 - 23,163,139 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC107959.4
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16570589
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.