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Human Genome Region MMP12

Assembly:
GRCh37.p11
Location:
chr11:102,702,497-102,822,936
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-305 Resolved There is a possible functional difference between the proteins encoded by RefSeq NM_002426.3 (MMP12) and the genomic region to which it aligns. PCR_RP11_AP000789_1 confirms the sequence of NM_002426 and has been included in the TPF as a contained product.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH159139.1 NW_003871077.1 FIX 120,441 1 1
           

MMP12 -- chr11 (NC_000011.9):102,702,497-102,822,936