Linked Data
dbSNP Id:
rs1579806752
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.53560625T>G , CM000667.2:g.53560625T>G | GRCh38 |
| NC_000005.9:g.52856455T>G , CM000667.1:g.52856455T>G | GRCh37 |
| NC_000005.8:g.52892212T>G | NCBI36 |
| NG_008200.1:g.4991T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011543414.1:c.-38T>G | XP_011541716.1:n.-38T>G | |
| XM_017009491.1:c.-38T>G | XP_016864980.1:n.-38T>G |