Canonical Allele Identifier:
CA2581616111
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.87942862T>G , CM000668.2:g.87942862T>G | GRCh38 |
| NC_000006.11:g.88652580T>G , CM000668.1:g.88652580T>G | GRCh37 |
| NC_000006.10:g.88709299T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001744246.1:n.1581T>G |