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Human Genome Region MMP28

Assembly:
GRCh37.p13
Location:
chr17:34,034,852-34,246,252
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-385 Resolved There is a possible functional difference between the proteins encoded by RefSeq NM_024302.3 (MMP28) and the genomic region to which it aligns. Switch points have been adjusted to use the sequence of AC015849.5, which contains the correct base, through the portion of the AC006237-AC015849 alignment containing this transcript discrepancy.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KB021646.2 NW_004166864.2 FIX 211,416 5 15
           

MMP28 -- chr17 (NC_000017.10):34,034,852-34,246,252