Canonical Allele Identifier:
CA1841175529
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551359C= , CM000671.2:g.25551359C= | GRCh38 |
| NC_000009.11:g.25551357C= , CM000671.1:g.25551357C= | GRCh37 |
| NC_000009.10:g.25541357C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-787G= | ||
| XR_929525.2:n.674-787G= |