Canonical Allele Identifier:
CA880474268
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.20217973C>A , CM000681.2:g.20217973C>A | GRCh38 |
| NC_000019.9:g.20328782C>A , CM000681.1:g.20328782C>A | GRCh37 |
| NC_000019.8:g.20189782C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936388.1:n.619-657G>T | ||
| XR_936389.1:n.502-657G>T | ||
| XR_936390.1:n.511-657G>T | ||
| XR_936391.1:n.514-657G>T | ||
| XR_936392.1:n.514-657G>T | ||
| XR_936394.1:n.41-761C>A | ||
| XR_001754063.2:n.1506-657G>T | ||
| XR_001754064.2:n.138-657G>T | ||
| XR_001754066.1:n.3912-657G>T | ||
| XR_001754067.1:n.3912-657G>T | ||
| XR_001754068.1:n.3912-657G>T | ||
| XR_936394.2:n.41-761C>A | ||
| XR_936406.2:n.1411-657G>T |