Linked Data
dbSNP Id:
rs1825907172
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22114930T>C , CM000671.2:g.22114930T>C | GRCh38 |
| NC_000009.11:g.22114929T>C , CM000671.1:g.22114929T>C | GRCh37 |
| NC_000009.10:g.22104929T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2908+1131T>C | ||
| NR_047532.1:n.1697+1131T>C | ||
| NR_047534.1:n.961+1131T>C | ||
| NR_047535.1:n.856+2535T>C | ||
| NR_047536.1:n.720+2535T>C | ||
| NR_047537.1:n.781-5270T>C | ||
| NR_047538.1:n.645-5270T>C | ||
| NR_047543.1:n.990+1131T>C | ||
| NR_120536.1:n.645-5574T>C |