Linked Data
dbSNP Id:
rs569604283
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22062250T>A , CM000671.2:g.22062250T>A | GRCh38 |
| NC_000009.11:g.22062249T>A , CM000671.1:g.22062249T>A | GRCh37 |
| NC_000009.10:g.22052249T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2158+224T>A | ||
| NR_047532.1:n.1075+5863T>A | ||
| NR_047533.1:n.644+13022T>A | ||
| NR_047534.1:n.644+13022T>A | ||
| NR_047535.1:n.780+5863T>A | ||
| NR_047536.1:n.644+13022T>A | ||
| NR_047537.1:n.780+5863T>A | ||
| NR_047538.1:n.644+13022T>A | ||
| NR_047539.1:n.2158+224T>A | ||
| NR_047540.1:n.854+224T>A | ||
| NR_047541.1:n.781-1694T>A | ||
| NR_047542.1:n.780+5863T>A | ||
| NR_047543.1:n.780+5863T>A | ||
| NR_120536.1:n.644+13022T>A |