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Chromosome X - NC_000023.11
Genomic Sequence: NC_000023.11 Chromosome X Reference GRCh38.p14 Primary Assembly NW_021160027.1 Chromosome X Reference GRCh38.p14 PATCHES NG_027735.1 RefSeqGene NC_060947.1 Chromosome X Alternate T2T-CHM13v2.0 NC_000023.10 Chromosome X Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
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.
NG_027735.1 RefSeqGene
NM_173571.2 → NP_775842.2 cancer/testis antigen 47A
See identical proteins and their annotated locations for NP_775842.2
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_000023.11 Reference GRCh38.p14 Primary Assembly
XM_011531319.3 → XP_011529621.1 cancer/testis antigen 47A isoform X1
See identical proteins and their annotated locations for XP_011529621.1
NW_021160027.1 Reference GRCh38.p14 PATCHES
NC_060947.1 Alternate T2T-CHM13v2.0
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