Linked Data
dbSNP Id:
rs1690138396
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202376314T>G , CM000664.2:g.202376314T>G | GRCh38 |
| NC_000002.11:g.203241037T>G , CM000664.1:g.203241037T>G | GRCh37 |
| NC_000002.10:g.202949282T>G | NCBI36 |
| NG_009363.1:g.4988T>G , LRG_712:g.4988T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011511687.1:c.-1161T>G | XP_011509989.1:n.-1161T>G | |
| XM_011511688.1:c.-1161T>G | XP_011509990.1:n.-1161T>G |