Linked Data
dbSNP Id:
rs1825906009
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22114886C>T , CM000671.2:g.22114886C>T | GRCh38 |
| NC_000009.11:g.22114885C>T , CM000671.1:g.22114885C>T | GRCh37 |
| NC_000009.10:g.22104885C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2908+1087C>T | ||
| NR_047532.1:n.1697+1087C>T | ||
| NR_047534.1:n.961+1087C>T | ||
| NR_047535.1:n.856+2491C>T | ||
| NR_047536.1:n.720+2491C>T | ||
| NR_047537.1:n.781-5314C>T | ||
| NR_047538.1:n.645-5314C>T | ||
| NR_047543.1:n.990+1087C>T | ||
| NR_120536.1:n.645-5618C>T |