Canonical Allele Identifier:
CA917965006
Gene:
Linked Data
dbSNP Id:
rs1562798421
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24283642_24283643insT , CM000669.2:g.24283642_24283643insT | GRCh38 |
| NC_000007.13:g.24323261_24323262insT , CM000669.1:g.24323261_24323262insT | GRCh37 |
| NC_000007.12:g.24289786_24289787insT | NCBI36 |
| NG_016148.1:g.4455_4456insT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_017012910.1:c.42-27944_42-27943insA | XP_016868399.1:n.42-27944_42-27943insA | |
| XM_017012911.1:c.42-27944_42-27943insA | XP_016868400.1:n.42-27944_42-27943insA | |
| XR_001745121.1:n.473+35714_473+35715insA | ||
| XR_001745122.1:n.345-86614_345-86613insA | ||
| XR_001745123.1:n.473+35714_473+35715insA | ||
| XR_001745124.1:n.473+35714_473+35715insA | ||
| XR_001745125.1:n.473+35714_473+35715insA | ||
| XR_001745126.1:n.473+35714_473+35715insA | ||
| XR_001745127.1:n.345-27944_345-27943insA | ||
| XR_001745129.1:n.473+35714_473+35715insA | ||
| XR_001745130.1:n.473+35714_473+35715insA | ||
| XR_001745131.1:n.473+35714_473+35715insA | ||
| XR_001745132.1:n.473+35714_473+35715insA |