Canonical Allele Identifier:
CA2611999027
Gene:
Linked Data
gnomAD v4:
11-2444563-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444563A>G , CM000673.2:g.2444563A>G | GRCh38 |
| NC_000011.9:g.2465793A>G , CM000673.1:g.2465793A>G | GRCh37 |
| NC_000011.8:g.2422369A>G | NCBI36 |
| NG_008935.1:g.4573A>G , LRG_287:g.4573A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930984.1:n.8T>C |