Canonical Allele Identifier:
CA2269954642
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63506330T= , CM000679.2:g.63506330T= | GRCh38 |
| NC_000017.10:g.61583691T= , CM000679.1:g.61583691T= | GRCh37 |
| NC_000017.9:g.58937423T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000577647.2:c.1970-726T= | ENSP00000464149.1:n.1970-726T= |