Canonical Allele Identifier:
CA1751305302
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.148560934C= , CM000669.2:g.148560934C= | GRCh38 |
| NC_000007.13:g.148258026C= , CM000669.1:g.148258026C= | GRCh37 |
| NC_000007.12:g.147888959C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_928099.1:n.300+7166G= | ||
| XR_928100.1:n.433+7166G= |