Linked Data
dbSNP Id:
rs1701646757
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.170813547T>G , CM000664.2:g.170813547T>G | GRCh38 |
| NC_000002.11:g.171670057T>G , CM000664.1:g.171670057T>G | GRCh37 |
| NC_000002.10:g.171378303T>G | NCBI36 |
| NG_021477.1:g.1858T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000454603.5:c.-64+125T>G | ENSP00000402366.1:n.-64+125T>G | |
| XM_011510922.1:c.-64+125T>G | XP_011509224.1:n.-64+125T>G |