Linked Data
dbSNP Id:
rs1848926771
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893847C>G , CM000673.2:g.14893847C>G | GRCh38 |
| NC_000011.9:g.14915393C>G , CM000673.1:g.14915393C>G | GRCh37 |
| NC_000011.8:g.14871969C>G | NCBI36 |
| NG_007936.1:g.3359G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011519898.1:c.-1603G>C | XP_011518200.1:n.-1603G>C | |
| XM_011519898.3:c.-1603G>C | XP_011518200.1:n.-1603G>C |