Canonical Allele Identifier:
CA2649624196
Gene:
Linked Data
gnomAD v4:
1-193121716-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121716C>T , CM000663.2:g.193121716C>T | GRCh38 |
| NC_000001.10:g.193090846C>T , CM000663.1:g.193090846C>T | GRCh37 |
| NC_000001.9:g.191357469C>T | NCBI36 |
| NG_012691.1:g.4759C>T , LRG_507:g.4759C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1941G>A |