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RASSF1-AS1 RASSF1 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 102060282, updated on 13-May-2022

Summary

Official Symbol
RASSF1-AS1provided by HGNC
Official Full Name
RASSF1 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:49091
See related
Ensembl:ENSG00000281358 AllianceGenome:HGNC:49091
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ANRASSF1
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Genomic context

See RASSF1-AS1 in Genome Data Viewer
Location:
3p21.31
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (50337511..50338300)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (50367234..50368024)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (50374942..50375731)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene hyaluronidase 2 Neighboring gene tumor suppressor 2, mitochondrial calcium regulator Neighboring gene Ras association domain family member 1 Neighboring gene zinc finger MYND-type containing 10 Neighboring gene NPR2 like, GATOR1 complex subunit

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

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.

RNA

  1. NR_109831.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC002481
    Related
    ENST00000629828.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    50337511..50338300
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    50367234..50368024
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)