Canonical Allele Identifier:
CA2593902008
Gene:
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.25551269A>T , CM000671.2:g.25551269A>T | GRCh38 |
| NC_000009.11:g.25551267A>T , CM000671.1:g.25551267A>T | GRCh37 |
| NC_000009.10:g.25541267A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929525.1:n.50-697T>A | ||
| XR_929525.2:n.674-697T>A |