Linked Data
dbSNP Id:
rs2131338166
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22088170G>T , CM000671.2:g.22088170G>T | GRCh38 |
| NC_000009.11:g.22088169G>T , CM000671.1:g.22088169G>T | GRCh37 |
| NC_000009.10:g.22078169G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2449-8202G>T | ||
| NR_047532.1:n.1076-4138G>T | ||
| NR_047534.1:n.645-9088G>T | ||
| NR_047535.1:n.781-24150G>T | ||
| NR_047536.1:n.645-24150G>T | ||
| NR_047537.1:n.780+31783G>T | ||
| NR_047538.1:n.645-32030G>T | ||
| NR_047543.1:n.781-24150G>T | ||
| NR_120536.1:n.645-32334G>T |