Human Genome Region B3GNTL1
- Assembly:
- GRCh38.p14
- Location:
- chr17:82,922,720-83,103,577
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270860.1 | NT_187612.1 | ALT | Unavailable | Unavailable | Unavailable | |