Linked Data
dbSNP Id:
rs1692378321
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.217041144A>C , CM000664.2:g.217041144A>C | GRCh38 |
| NC_000002.11:g.217905867A>C , CM000664.1:g.217905867A>C | GRCh37 |
| NC_000002.10:g.217614112A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_923881.1:n.299+47126A>C | ||
| XR_923883.1:n.294+47126A>C | ||
| XR_923885.1:n.862+47126A>C | ||
| XR_923886.1:n.359-14047A>C | ||
| XR_923887.1:n.300-14047A>C | ||
| XR_001739169.1:n.11844+47126A>C | ||
| XR_001739170.2:n.8480+47126A>C | ||
| XR_001739171.2:n.8347+47126A>C | ||
| XR_923878.2:n.7457A>C |