Canonical Allele Identifier:
CA1915219148
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.63898984T= , CM000672.2:g.63898984T= | GRCh38 |
| NC_000010.10:g.65658744T= , CM000672.1:g.65658744T= | GRCh37 |
| NC_000010.9:g.65328750T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_946010.1:n.275+11308T= | ||
| XR_946011.1:n.275+11308T= | ||
| XR_946012.1:n.275+11308T= | ||
| XR_946013.1:n.275+11308T= |