Canonical Allele Identifier:
CA2193710256
Gene:
Linked Data
dbSNP Id:
rs1895000818
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.87419311_87419322del , CM000677.2:g.87419311_87419322del | GRCh38 |
| NC_000015.9:g.87962542_87962553del , CM000677.1:g.87962542_87962553del | GRCh37 |
| NC_000015.8:g.85763546_85763557del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932584.1:n.340-51_340-40del | ||
| XR_932585.1:n.340-51_340-40del | ||
| XR_001751647.1:n.617-51_617-40del | ||
| XR_932585.2:n.627-51_627-40del |