Human Genome Region UGT2B17
- Assembly:
- GRCh37.p13
- Location:
- chr4:69,170,077-69,878,175
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL000257.1 | NT_167250.1 | ALT | 590,426 | 725 | 157 | |