Skip navigation and go to main content

Human Genome Region MAPT

Assembly:
GRCh37
Location:
chr17:43,384,864-44,913,631
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL000258.1 NT_167251.1 ALT 1,680,828 11,651 679,402
           

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