Canonical Allele Identifier:
CA1392628849
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.109743515T= , CM000665.2:g.109743515T= | GRCh38 |
| NC_000003.11:g.109462362T= , CM000665.1:g.109462362T= | GRCh37 |
| NC_000003.10:g.110945052T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924325.1:n.142+63320T= |