Linked Data
dbSNP Id:
rs1691491528
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216998694A>G , CM000664.2:g.216998694A>G | GRCh38 |
| NC_000002.11:g.217863417A>G , CM000664.1:g.217863417A>G | GRCh37 |
| NC_000002.10:g.217571662A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923881.1:n.299+4676A>G | ||
| XR_923883.1:n.294+4676A>G | ||
| XR_923885.1:n.862+4676A>G | ||
| XR_923886.1:n.300-2353A>G | ||
| XR_923887.1:n.299+4676A>G | ||
| XR_001739169.1:n.11844+4676A>G | ||
| XR_001739170.2:n.8480+4676A>G | ||
| XR_001739171.2:n.8347+4676A>G |