Linked Data
gnomAD v4:
22-21658235-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658235C>T , CM000684.2:g.21658235C>T | GRCh38 |
| NC_000022.10:g.22012524C>T , CM000684.1:g.22012524C>T | GRCh37 |
| NC_000022.9:g.20342524C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.163-31C>T | ||
| ENST00000498589.1:n.343-31C>T | ||
| XM_017029165.1:c.478-31C>T | XP_016884654.1:n.478-31C>T | |
| NR_169729.1:n.1047C>T | ||
| NR_169730.1:n.950C>T | ||
| NR_169731.1:n.432-2602C>T | ||
| NR_169732.1:n.132-31C>T | ||
| NR_169733.1:n.214-55C>T | ||
| NR_169734.1:n.214-31C>T |