Canonical Allele Identifier:
CA13754591
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.50761880C>T , CM000674.2:g.50761880C>T | GRCh38 |
| NC_000012.11:g.51155663C>T , CM000674.1:g.51155663C>T | GRCh37 |
| NC_000012.10:g.49441930C>T | NCBI36 |
| NG_027673.1:g.2875C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_944956.1:n.1087+594G>A |