Canonical Allele Identifier:
CA2581381477
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521955C>A , CM000681.2:g.33521955C>A | GRCh38 |
| NC_000019.9:g.34012861C>A , CM000681.1:g.34012861C>A | GRCh37 |
| NC_000019.8:g.38704701C>A | NCBI36 |
| NG_013358.1:g.4939G>T | |
| NG_013358.2:g.4939G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.14C>A | ||
| XR_935919.1:n.9C>A | ||
| XR_001754035.2:n.22C>A | ||
| XR_935918.2:n.22C>A |