Linked Data
dbSNP Id:
rs1824929560
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22088180T>G , CM000671.2:g.22088180T>G | GRCh38 |
| NC_000009.11:g.22088179T>G , CM000671.1:g.22088179T>G | GRCh37 |
| NC_000009.10:g.22078179T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2449-8192T>G | ||
| NR_047532.1:n.1076-4128T>G | ||
| NR_047534.1:n.645-9078T>G | ||
| NR_047535.1:n.781-24140T>G | ||
| NR_047536.1:n.645-24140T>G | ||
| NR_047537.1:n.780+31793T>G | ||
| NR_047538.1:n.645-32020T>G | ||
| NR_047543.1:n.781-24140T>G | ||
| NR_120536.1:n.645-32324T>G |