Linked Data
dbSNP Id:
rs1823813983
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22061423_22061424del , CM000671.2:g.22061423_22061424del | GRCh38 |
| NC_000009.11:g.22061422_22061423del , CM000671.1:g.22061422_22061423del | GRCh37 |
| NC_000009.10:g.22051422_22051423del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2085-530_2085-529del | ||
| NR_047532.1:n.1075+5036_1075+5037del | ||
| NR_047533.1:n.644+12195_644+12196del | ||
| NR_047534.1:n.644+12195_644+12196del | ||
| NR_047535.1:n.780+5036_780+5037del | ||
| NR_047536.1:n.644+12195_644+12196del | ||
| NR_047537.1:n.780+5036_780+5037del | ||
| NR_047538.1:n.644+12195_644+12196del | ||
| NR_047539.1:n.2085-530_2085-529del | ||
| NR_047540.1:n.781-530_781-529del | ||
| NR_047541.1:n.781-2521_781-2520del | ||
| NR_047542.1:n.780+5036_780+5037del | ||
| NR_047543.1:n.780+5036_780+5037del | ||
| NR_120536.1:n.644+12195_644+12196del |