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Gene: AC037441.1 (novel transcript) Homo sapiens
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Symbol: AC037441.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101929237; uncharacterized LOC101929237
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl822,877,972 - 22,888,022 (+)EnsemblGRCh38hg38GRCh38
GRCh38822,877,972 - 22,888,022 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37822,735,497 - 22,745,535 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p21.3NCBI
HuRef821,279,479 - 21,289,682 (+)NCBIHuRef
CHM1_1822,937,740 - 22,947,790 (+)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 AC037441.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16558253
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.