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Human Genome Issue HG-348

GeneID: 10929 (SFRS2B), poor quality (includes component misassembly)
There is a possible functional difference between the proteins encoded by RefSeq NM_032102.2 (SFRS2B) and the genomic region to which it aligns.
Resolved (GRC Resolved by Experimental Method)
Clone Problem
Last updated:
Experiment type:
Affects version:
Fix version:
GRCh37.p6, GRCh37.p7
PCR_RP11_AP001264_1 confirms the sequence of NM_032102 and has been included in the TPF as a contained product.

Patches and alternate loci

Scaffold type:
FIX patch to GRCh37
This sequence will be incorporated into the reference assembly in the next major assembly release. At that time, the accession number for this patch will be made secondary to the reference chromosome accession. This patch contains FP929014.1, which has been used to correct a 1 nt deletion in NC_000011.9 component AP001264.4 that affects representation of SFRS2B (NM_032102.2). It also contains FP884233.1, which has been used to correct a 1 nt deletion in component AP002383.3 affecting representation of CWC15 (NM_016403.3).
Revision history of patches and alts for HG-348
Assembly Scaffold type Contig name GenBank accession RefSeq accession Region
GRCh37.p6 FIX HG348_PATCH JH159141.1 NW_003871079.1 SRSF8
GRCh37.p7 FIX HG348_PATCH JH159141.2 NW_003871079.1 CWC15_SRSF8

Locations and genomic context

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  • (View region: Ensembl | NCBI | UCSC)
  • (View region: Ensembl | NCBI | UCSC)