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Human Genome Region B3GNT6

Assembly:
GRCh37.p11
Location:
chr11:76,709,408-76,900,812
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-414 Resolved There is a possible functional difference between the proteins encoded by RefSeq NM_138706.3 (B3GNT6) and the genomic region to which it aligns. PCR_RP11_AP000752_1 confirms the sequence of NM_138706 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
JH159143.1 NW_003871081.1 FIX 191,402 1 0
           

B3GNT6 -- chr11 (NC_000011.9):76,709,408-76,900,812