Linked Data
dbSNP Id:
rs111248552
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43337790T>G , CM000663.2:g.43337790T>G | GRCh38 |
| NC_000001.10:g.43803461T>G , CM000663.1:g.43803461T>G | GRCh37 |
| NC_000001.9:g.43576048T>G | NCBI36 |
| NG_007525.1:g.4987T>G , LRG_510:g.4987T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011541478.1:c.-59T>G | XP_011539780.1:n.-59T>G | |
| XM_017001320.1:c.-59T>G | XP_016856809.1:n.-59T>G |