Linked Data
dbSNP Id:
rs1657749275
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207453960T>G , CM000663.2:g.207453960T>G | GRCh38 |
| NC_000001.10:g.207627305T>G , CM000663.1:g.207627305T>G | GRCh37 |
| NC_000001.9:g.205693928T>G | NCBI36 |
| NG_013006.1:g.4661T>G , LRG_348:g.4661T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699640.1:c.-385+865T>G | ENSP00000514493.1:n.-385+865T>G |