Canonical Allele Identifier:
CA1300258753
Gene:
Linked Data
dbSNP Id:
rs1683146007
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.155870513dup , CM000664.2:g.155870513dup | GRCh38 |
| NC_000002.11:g.156727025dup , CM000664.1:g.156727025dup | GRCh37 |
| NC_000002.10:g.156435271dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923501.1:n.320-3326dup | ||
| XR_001739749.1:n.331-29529dup | ||
| XR_001739750.1:n.331-29529dup | ||
| XR_001739751.1:n.331-29529dup | ||
| XR_923501.2:n.331-3326dup |