Canonical Allele Identifier:
CA1691656466
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17957915A= , CM000669.2:g.17957915A= | GRCh38 |
| NC_000007.13:g.17997538A= , CM000669.1:g.17997538A= | GRCh37 |
| NC_000007.12:g.17964063A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927078.1:n.271-755A= |