Linked Data
gnomAD v4:
22-21658224-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658224C>T , CM000684.2:g.21658224C>T | GRCh38 |
| NC_000022.10:g.22012513C>T , CM000684.1:g.22012513C>T | GRCh37 |
| NC_000022.9:g.20342513C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.163-42C>T | ||
| ENST00000498589.1:n.343-42C>T | ||
| XM_017029165.1:c.478-42C>T | XP_016884654.1:n.478-42C>T | |
| NR_169729.1:n.1036C>T | ||
| NR_169730.1:n.939C>T | ||
| NR_169731.1:n.432-2613C>T | ||
| NR_169732.1:n.132-42C>T | ||
| NR_169733.1:n.214-66C>T | ||
| NR_169734.1:n.214-42C>T |