Linked Data
dbSNP Id:
rs1848921638
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893504T>C , CM000673.2:g.14893504T>C | GRCh38 |
| NC_000011.9:g.14915050T>C , CM000673.1:g.14915050T>C | GRCh37 |
| NC_000011.8:g.14871626T>C | NCBI36 |
| NG_007936.1:g.3702A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.1:c.-1260A>G | XP_011518200.1:n.-1260A>G | |
| XM_011519898.3:c.-1260A>G | XP_011518200.1:n.-1260A>G |