Homo sapiens unplaced genomic scaffold, GRCh38.p14 Primary Assembly HS - Nucleotide

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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...
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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...

Assembly
Assembly
BioProject
Related BioProject entry
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Components (Core)
Links to Core components
dbVar
Link from Nucleotide to dbVar
Gene
Link to related Genes
Identical GenBank Sequence
Links from RefSeq assemblies to source GenBank records.
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.
SNP
Related SNPs

Homo sapiens unplaced genomic scaffold, GRCh38.p14 Primary Assembly HSCHRUN_RAND...
Homo sapiens unplaced genomic scaffold, GRCh38.p14 Primary Assembly HSCHRUN_RANDOM_124
gi|568801882|gnl|ASM:GCF_000001305. CHRUN_RANDOM_124|ref|NT_187420.1||gpp|GPS_003205808.1|

Nucleotide

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Nucleotide