Canonical Allele Identifier:
CA1691656468
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17957919C= , CM000669.2:g.17957919C= | GRCh38 |
| NC_000007.13:g.17997542C= , CM000669.1:g.17997542C= | GRCh37 |
| NC_000007.12:g.17964067C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927078.1:n.271-751C= |