Canonical Allele Identifier:
CA1841175699
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551607T= , CM000671.2:g.25551607T= | GRCh38 |
| NC_000009.11:g.25551605T= , CM000671.1:g.25551605T= | GRCh37 |
| NC_000009.10:g.25541605T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-1035A= | ||
| XR_929525.2:n.674-1035A= |