Linked Data
dbSNP Id:
rs907786268
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22116097T>C , CM000671.2:g.22116097T>C | GRCh38 |
| NC_000009.11:g.22116096T>C , CM000671.1:g.22116096T>C | GRCh37 |
| NC_000009.10:g.22106096T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2908+2298T>C | ||
| NR_047532.1:n.1697+2298T>C | ||
| NR_047534.1:n.961+2298T>C | ||
| NR_047535.1:n.857-2547T>C | ||
| NR_047536.1:n.721-2547T>C | ||
| NR_047537.1:n.781-4103T>C | ||
| NR_047538.1:n.645-4103T>C | ||
| NR_047543.1:n.990+2298T>C | ||
| NR_120536.1:n.645-4407T>C |