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Chromosome 11 - NC_000011.10
Genomic Sequence: NC_000011.10 Chromosome 11 Reference GRCh38.p14 Primary Assembly NC_060935.1 Chromosome 11 Alternate T2T-CHM13v2.0 NC_000011.9 Chromosome 11 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
See all (295) citations in PubMed
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)
Go to the HIV-1, Human Interaction Database
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_003146.3 → NP_003137.1 FACT complex subunit SSRP1
See identical proteins and their annotated locations for NP_003137.1
Status: REVIEWED
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_000011.10 Reference GRCh38.p14 Primary Assembly
XM_047427498.1 → XP_047283454.1 FACT complex subunit SSRP1 isoform X2
XM_017018180.2 → XP_016873669.2 FACT complex subunit SSRP1 isoform X1
XM_047427499.1 → XP_047283455.1 FACT complex subunit SSRP1 isoform X3
NC_060935.1 Alternate T2T-CHM13v2.0
XM_054369757.1 → XP_054225732.1 FACT complex subunit SSRP1 isoform X2
XM_054369756.1 → XP_054225731.1 FACT complex subunit SSRP1 isoform X1
XM_054369758.1 → XP_054225733.1 FACT complex subunit SSRP1 isoform X3
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