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Human Genome Region APOB

Assembly:
GRCh38.p14
Location:
chr2:20,949,331-21,194,057
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
MU273344.1 Not yet assigned FIX Unavailable Unavailable Unavailable
           

APOB -- chr2 (CM000664.2):20,949,331-21,194,057