Linked Data
dbSNP Id:
rs1902058729
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173493del , CM000678.2:g.173493del | GRCh38 |
| NC_000016.9:g.223492del , CM000678.1:g.223492del | GRCh37 |
| NC_000016.8:g.163492del | NCBI36 |
| NG_000006.1:g.34356del | |
| NG_059186.1:g.1843del | |
| NG_059271.1:g.5647del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000251595.11:c.322del MANE Select | ENSP00000251595.6:p.Val108Ter | |
| ENST00000251595.10:c.322del | ENSP00000251595.6:p.Val108Ter | |
| ENST00000397806.1:c.226del | ENSP00000380908.1:p.Val76Ter | |
| ENST00000482565.1:n.458del | ||
| NM_000517.4:c.322del | NP_000508.1:p.Val108Ter | |
| NM_000517.6:c.322del MANE Select | NP_000508.1:p.Val108Ter |