Canonical Allele Identifier:
CA2659994680
Gene:
Linked Data
gnomAD v4:
2-88016275-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016275T>C , CM000664.2:g.88016275T>C | GRCh38 |
| NC_000002.11:g.88315794T>C , CM000664.1:g.88315794T>C | GRCh37 |
| NC_000002.10:g.88096909T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.620T>C | ||
| XR_940336.3:n.620T>C |