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Homo sapiens chromosome 17 genomic patch of type NOVEL, GRCh38.p14 PATCHES HSCHR17_13_CTG4

NCBI Reference Sequence: NW_025791801.1

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    Find regions of similarity between this sequence and other sequences using BLAST.
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    Design and test primers for this sequence using Primer-BLAST.
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    Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
  • Find in this Sequence
    Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...

Related information

  • Assembly
    Assembly
  • BioProject
    Related BioProject entry
  • Protein
    Protein sequence from Nucleotide coding region
  • Taxonomy
    Taxonomy sequences associated with Nucleotide record
  • Components (Core)
    Links to Core components
  • Gene
    Link to related Genes
  • Identical GenBank Sequence
    Links from RefSeq assemblies to source GenBank records.
  • PubMed (Weighted)
    Links to pubmed
  • RNA
    RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.

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