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Human Genome Region TRIM69

Assembly:
GRCh38.p14
Location:
chr15:44,676,664-44,913,053
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270849.1 NT_187605.1 ALT Unavailable Unavailable Unavailable
           

TRIM69 -- chr15 (CM000677.2):44,676,664-44,913,053