Canonical Allele Identifier:
CA2197910487
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.96104564T>C , CM000677.2:g.96104564T>C | GRCh38 |
| NC_000015.9:g.96647793T>C , CM000677.1:g.96647793T>C | GRCh37 |
| NC_000015.8:g.94448797T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932658.1:n.314-406A>G | ||
| NR_158193.1:n.1087-406A>G | ||
| XR_001751686.2:n.138-406A>G | ||
| XR_002957737.1:n.450+113680T>C |