Linked Data
dbSNP Id:
rs1268477798
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22088217G>T , CM000671.2:g.22088217G>T | GRCh38 |
| NC_000009.11:g.22088216G>T , CM000671.1:g.22088216G>T | GRCh37 |
| NC_000009.10:g.22078216G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2449-8155G>T | ||
| NR_047532.1:n.1076-4091G>T | ||
| NR_047534.1:n.645-9041G>T | ||
| NR_047535.1:n.781-24103G>T | ||
| NR_047536.1:n.645-24103G>T | ||
| NR_047537.1:n.780+31830G>T | ||
| NR_047538.1:n.645-31983G>T | ||
| NR_047543.1:n.781-24103G>T | ||
| NR_120536.1:n.645-32287G>T |