Canonical Allele Identifier:
CA2713119486
Gene:
Linked Data
dbSNP Id:
rs150864894
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812332_155812333dup , CM000668.2:g.155812332_155812333dup | GRCh38 |
| NC_000006.11:g.156133466_156133467dup , CM000668.1:g.156133466_156133467dup | GRCh37 |
| NC_000006.10:g.156175158_156175159dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+18913_79+18914dup | ||
| XR_943146.1:n.645-293_645-292dup | ||
| XR_001744423.1:n.699-293_699-292dup | ||
| XR_001744424.1:n.79+18913_79+18914dup |