Human Genome Region TMEM50B
- Assembly:
- GRCh38.p14
- Location:
- chr21:33,405,429-33,512,559
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| GL383581.2 | NW_003315970.2 | ALT | Unavailable | Unavailable | Unavailable | |