Canonical Allele Identifier:
CA1870932951
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.108092825T= , CM000671.2:g.108092825T= | GRCh38 |
| NC_000009.11:g.110855106T= , CM000671.1:g.110855106T= | GRCh37 |
| NC_000009.10:g.109894927T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930239.1:n.461-39531A= | ||
| XR_001746881.1:n.668-39531A= | ||
| XR_001746882.1:n.668-39531A= |