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Region information for MAPT

Organism:
Human
Assembly:
GRCh37.p13
Region:
chr17:43,384,864-44,913,631
Cytogenetic location:

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Issue information
JIRA ticket ID Status Description Resolution text
HG-1448 Resolved There is a type 2 gap between AC217768.1 and AC139677.4 in alt locus NT_167251.1 originally described in HG-1146. This duplicate Jira issue is being used to manage an update at this gap that is being considered for patch release. There is a type 2 gap between AC217768.1 and AC139677.4 in alt locus NT_167251.1 originally described in HG-1146. This duplicate Jira issue is being used to manage an update at this gap that is being considered for patch release.
Sequence information
GenBank ID RefSeq ID Sequence Type Length Alignment mismatch Unique sequence Show in Viewer
GL000258.1 NT_167251.1 Alternate locus 1,680,828 13,849 203,551
JH720447.1 NW_003871086.1 Fix 454,385 846 225,346
           

chr17 (NC_000017.10):43,384,864-44,913,631