Canonical Allele Identifier:
CA2129379020
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36384768_36384769delinsCT , CM000676.2:g.36384768_36384769delinsCT | GRCh38 |
| NC_000014.8:g.36853973_36853974delinsCT , CM000676.1:g.36853973_36853974delinsCT | GRCh37 |
| NC_000014.7:g.35923724_35923725delinsCT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537428.1:c.319-12391_319-12390delinsCT | XP_011535730.1:n.319-12391_319-12390delinsCT | |
| XR_943756.1:n.358+23672_358+23673delinsCT |