Canonical Allele Identifier:
CA917896344
Gene:
Linked Data
dbSNP Id:
rs1583057153
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812558dup , CM000668.2:g.155812558dup | GRCh38 |
| NC_000006.11:g.156133692dup , CM000668.1:g.156133692dup | GRCh37 |
| NC_000006.10:g.156175384dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19139dup | ||
| XR_943146.1:n.645-518dup | ||
| XR_001744423.1:n.699-518dup | ||
| XR_001744424.1:n.79+19139dup |