Canonical Allele Identifier:
CA2581691878
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.147754660G>T , CM000663.2:g.147754660G>T | GRCh38 |
| NG_009369.2:g.23715C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922078.1:n.434-22901G>T | ||
| XR_922079.1:n.434-22901G>T | ||
| XR_922079.3:n.744-22901G>T |