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Human Genome Region SLC37A4

Assembly:
GRCh37.p13
Location:
chr11:118,849,111-118,957,986
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-299 Reopened There is a possible functional difference between the proteins encoded by RefSeq NM_001467.4 (SLC37A4) and the genomic region to which it aligns. PCR_RP11_AP003392_1 (FP885832.1) confirms the sequence of NM_001467 and has been included in the TPF as a contained product. This component has subsequently been replaced by FO680690.4.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH159138.1 NW_003871076.1 FIX 108,875 0 0
           

SLC37A4 -- chr11 (NC_000011.9):118,849,111-118,957,986