Canonical Allele Identifier:
CA1369169841
Gene:
Linked Data
dbSNP Id:
rs2041752853
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428061dup , CM000665.2:g.61428061dup | GRCh38 |
| NC_000003.11:g.61413735dup , CM000665.1:g.61413735dup | GRCh37 |
| NC_000003.10:g.61388775dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-375dup | ||
| XR_940893.1:n.164+453dup | ||
| XR_001740725.1:n.202+453dup | ||
| XR_940892.2:n.203-375dup |