Homo sapiens chromosome 5 genomic patch of type NOVEL, GRCh38.p14 PATC - Nucleotide

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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
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Protein
Protein sequence from Nucleotide coding region
Taxonomy
Taxonomy sequences associated with Nucleotide record
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Links from RefSeq assemblies to source GenBank records.
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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.

Homo sapiens chromosome 5 genomic patch of type NOVEL, GRCh38.p14 PATCHES HSCHR5...
Homo sapiens chromosome 5 genomic patch of type NOVEL, GRCh38.p14 PATCHES HSCHR5_10_CTG1
gi|2190932338|gnl|ASM:GCF_000005045 SCHR5_10_CTG1|ref|NW_025791779.1||gpp|GPS_022396411.1|

Nucleotide

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Nucleotide