Canonical Allele Identifier:
CA1968513029
Gene:
Linked Data
dbSNP Id:
rs1856778509
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45506571del , CM000673.2:g.45506571del | GRCh38 |
| NC_000011.9:g.45528121del , CM000673.1:g.45528121del | GRCh37 |
| NC_000011.8:g.45484697del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001748204.2:n.909-16798del | ||
| XR_931245.3:n.566-16798del |