Canonical Allele Identifier:
CA2210934398
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17968279C= , CM000678.2:g.17968279C= | GRCh38 |
| NC_000016.9:g.18062136C= , CM000678.1:g.18062136C= | GRCh37 |
| NC_000016.8:g.17969637C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001752092.2:n.260-591G= | ||
| XR_001752093.1:n.260-591G= |