Canonical Allele Identifier:
CA2611999008
Gene:
Linked Data
gnomAD v4:
11-2444550-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444550C>A , CM000673.2:g.2444550C>A | GRCh38 |
| NC_000011.9:g.2465780C>A , CM000673.1:g.2465780C>A | GRCh37 |
| NC_000011.8:g.2422356C>A | NCBI36 |
| NG_008935.1:g.4560C>A , LRG_287:g.4560C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930984.1:n.21G>T |