Linked Data
dbSNP Id:
rs2157719
gnomAD v2:
9-22033366-C-T
gnomAD v3:
9-22033367-C-T
gnomAD v4:
9-22033367-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22033367C>T , CM000671.2:g.22033367C>T | GRCh38 |
| NC_000009.11:g.22033366C>T , CM000671.1:g.22033366C>T | GRCh37 |
| NC_000009.10:g.22023366C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.846+381C>T | ||
| NR_047532.1:n.533+3773C>T | ||
| NR_047533.1:n.372-13384C>T | ||
| NR_047534.1:n.372-13384C>T | ||
| NR_047535.1:n.372-13384C>T | ||
| NR_047536.1:n.372-13384C>T | ||
| NR_047537.1:n.372-13384C>T | ||
| NR_047538.1:n.372-13384C>T | ||
| NR_047539.1:n.846+381C>T | ||
| NR_047540.1:n.372-13384C>T | ||
| NR_047541.1:n.372-13384C>T | ||
| NR_047542.1:n.372-13384C>T | ||
| NR_047543.1:n.372-13384C>T | ||
| NR_120536.1:n.372-13384C>T |