Canonical Allele Identifier:
CA1723810369
Gene:
Linked Data
dbSNP Id:
rs1840054802
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87913768_87913770dup , CM000669.2:g.87913768_87913770dup | GRCh38 |
| NC_000007.13:g.87543083_87543085dup , CM000669.1:g.87543083_87543085dup | GRCh37 |
| NC_000007.12:g.87381019_87381021dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927723.1:n.148+131_148+133dup | ||
| XR_927724.1:n.192+131_192+133dup |