Homo sapiens chromosome 12 genomic patch of type NOVEL, GRCh38.p14 PAT - 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...

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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 12 genomic patch of type NOVEL, GRCh38.p14 PATCHES HSCHR...
Homo sapiens chromosome 12 genomic patch of type NOVEL, GRCh38.p14 PATCHES HSCHR12_8_CTG2_1
gi|1208651584|gnl|ASM:GCF_000005045 SCHR12_8_CTG2_1|ref|NW_018654720.1|

Nucleotide

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Nucleotide