Linked Data
dbSNP Id:
rs1198286651
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22062080_22062082del , CM000671.2:g.22062080_22062082del | GRCh38 |
| NC_000009.11:g.22062079_22062081del , CM000671.1:g.22062079_22062081del | GRCh37 |
| NC_000009.10:g.22052079_22052081del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2158+54_2158+56del | ||
| NR_047532.1:n.1075+5693_1075+5695del | ||
| NR_047533.1:n.644+12852_644+12854del | ||
| NR_047534.1:n.644+12852_644+12854del | ||
| NR_047535.1:n.780+5693_780+5695del | ||
| NR_047536.1:n.644+12852_644+12854del | ||
| NR_047537.1:n.780+5693_780+5695del | ||
| NR_047538.1:n.644+12852_644+12854del | ||
| NR_047539.1:n.2158+54_2158+56del | ||
| NR_047540.1:n.854+54_854+56del | ||
| NR_047541.1:n.781-1864_781-1862del | ||
| NR_047542.1:n.780+5693_780+5695del | ||
| NR_047543.1:n.780+5693_780+5695del | ||
| NR_120536.1:n.644+12852_644+12854del |