Canonical Allele Identifier:
CA1563552032
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.92222673A= , CM000667.2:g.92222673A= | GRCh38 |
| NC_000005.9:g.91518490A= , CM000667.1:g.91518490A= | GRCh37 |
| NC_000005.8:g.91554246A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948565.1:n.394+17989A= |