Canonical Allele Identifier:
CA1901525469
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.34998722T= , CM000672.2:g.34998722T= | GRCh38 |
| NC_000010.10:g.35287650T= , CM000672.1:g.35287650T= | GRCh37 |
| NC_000010.9:g.35327656T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930817.1:n.509-4360A= |