Human Genome Region MUCIN_REGION_2
- Assembly:
- GRCh38.p14
- Location:
- chr3:195,629,504-195,827,492
- Cytogenetic location:
No associated genome issues
| Show in Viewer | GenBank ID | RefSeq ID | Scaffold type | Length | Alignment mismatch | Unique sequence |
|---|---|---|---|---|---|---|
| KI270779.1 | NT_187532.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270895.1 | NT_187649.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270924.1 | NT_187678.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270934.1 | NT_187688.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270935.1 | NT_187689.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270936.1 | NT_187690.1 | ALT | Unavailable | Unavailable | Unavailable | |
| KI270937.1 | NT_187691.1 | ALT | Unavailable | Unavailable | Unavailable | |