PREDICTED: Homo sapiens FA complementation group B (FANCB), transcript - 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...
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Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

RefSeq protein product
See the reference protein sequence for Fanconi anemia group B protein isoform X2 (XP_047297878.1).

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Protein
Protein sequence from Nucleotide coding region
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Taxonomy sequences associated with Nucleotide record
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Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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PREDICTED: Homo sapiens FA complementation group B (FANCB), transcript variant X...
PREDICTED: Homo sapiens FA complementation group B (FANCB), transcript variant X8, mRNA
gi|2217391379|ref|XM_047441922.1|

Nucleotide

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Nucleotide