Linked Data
gnomAD v4:
22-21658608-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658608G>T , CM000684.2:g.21658608G>T | GRCh38 |
| NC_000022.10:g.22012897G>T , CM000684.1:g.22012897G>T | GRCh37 |
| NC_000022.9:g.20342897G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.286+219G>T | ||
| ENST00000498589.1:n.540-35G>T | ||
| XM_017029165.1:c.674+146G>T | XP_016884654.1:n.674+146G>T | |
| NR_169729.1:n.1420G>T | ||
| NR_169730.1:n.1323G>T | ||
| NR_169731.1:n.432-2229G>T | ||
| NR_169732.1:n.328+146G>T | ||
| NR_169733.1:n.387-35G>T | ||
| NR_169734.1:n.411-35G>T |