Canonical Allele Identifier:
CA1940853889
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.121141109C= , CM000672.2:g.121141109C= | GRCh38 |
| NC_000010.10:g.122900623C= , CM000672.1:g.122900623C= | GRCh37 |
| NC_000010.9:g.122890613C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_946379.1:n.286-10939C= | |
| XR_946379.2:n.357-10939C= |