Canonical Allele Identifier:
CA919823932
Gene:
Linked Data
dbSNP Id:
rs1555592690
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237299_30237342del , CM000679.2:g.30237299_30237342del | GRCh38 |
| NC_000017.10:g.28564317_28564360del , CM000679.1:g.28564317_28564360del | GRCh37 |
| NC_000017.9:g.25588443_25588486del | NCBI36 |
| NG_011747.2:g.3599_3642del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_934654.1:n.165+229_165+272del | ||
| XR_001752824.1:n.280+229_280+272del |