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Chromosome 16 - NC_000016.10
Genomic Sequence: NC_000016.10 Chromosome 16 Reference GRCh38.p14 Primary Assembly NC_060940.1 Chromosome 16 Alternate T2T-CHM13v2.0 NC_000016.9 Chromosome 16 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
Find tests for this gene in the NIH Genetic Testing Registry (GTR)
Review eQTL and phenotype association data in this region using PheGenI
See variants in ClinVar
See studies and variants in dbVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
NEW Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.
NM_001012984.3 → NP_001013002.2 uncharacterized protein C16orf86
See identical proteins and their annotated locations for NP_001013002.2
Status: VALIDATED
The following sections contain reference sequences that belong to a specific genome build. Explain
This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.
NC_000016.10 Reference GRCh38.p14 Primary Assembly
XM_047434097.1 → XP_047290053.1 uncharacterized protein C16orf86 isoform X1
XM_047434098.1 → XP_047290054.1 uncharacterized protein C16orf86 isoform X2
XM_005255952.6 → XP_005256009.1 uncharacterized protein C16orf86 isoform X3
NC_060940.1 Alternate T2T-CHM13v2.0
XM_054380314.1 → XP_054236289.1 uncharacterized protein C16orf86 isoform X3
XM_054380312.1 → XP_054236287.1 uncharacterized protein C16orf86 isoform X1
XM_054380313.1 → XP_054236288.1 uncharacterized protein C16orf86 isoform X2
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