Canonical Allele Identifier:
CA10780597
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.147754660G= , CM000663.2:g.147754660G= | GRCh38 |
| NG_009369.2:g.23715C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922078.1:n.434-22901G= | ||
| XR_922079.1:n.434-22901G= | ||
| XR_922079.3:n.744-22901G= |