Canonical Allele Identifier:
CA918357099
Gene:
Linked Data
dbSNP Id:
rs1586448148
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.122395750_122395751insT , CM000670.2:g.122395750_122395751insT | GRCh38 |
| NC_000008.10:g.123407989_123407990insT , CM000670.1:g.123407989_123407990insT | GRCh37 |
| NC_000008.9:g.123477170_123477171insT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928599.1:n.152+3421_152+3422insA | ||
| XR_928599.3:n.152+3421_152+3422insA |