Canonical Allele Identifier:
CA1870933022
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.108092969T= , CM000671.2:g.108092969T= | GRCh38 |
| NC_000009.11:g.110855250T= , CM000671.1:g.110855250T= | GRCh37 |
| NC_000009.10:g.109895071T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_930239.1:n.461-39675A= | ||
| XR_001746881.1:n.668-39675A= | ||
| XR_001746882.1:n.668-39675A= |