Canonical Allele Identifier:
CA2699703487
Gene:
Linked Data
dbSNP Id:
rs1293401562
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016270del , CM000664.2:g.88016270del | GRCh38 |
| NC_000002.11:g.88315789del , CM000664.1:g.88315789del | GRCh37 |
| NC_000002.10:g.88096904del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.615del | ||
| XR_940336.3:n.615del |