Linked Data
dbSNP Id:
rs2131370852
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22114535T>C , CM000671.2:g.22114535T>C | GRCh38 |
| NC_000009.11:g.22114534T>C , CM000671.1:g.22114534T>C | GRCh37 |
| NC_000009.10:g.22104534T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2908+736T>C | ||
| NR_047532.1:n.1697+736T>C | ||
| NR_047534.1:n.961+736T>C | ||
| NR_047535.1:n.856+2140T>C | ||
| NR_047536.1:n.720+2140T>C | ||
| NR_047537.1:n.781-5665T>C | ||
| NR_047538.1:n.645-5665T>C | ||
| NR_047543.1:n.990+736T>C | ||
| NR_120536.1:n.645-5969T>C |