Linked Data
dbSNP Id:
rs1411159252
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207453944G>A , CM000663.2:g.207453944G>A | GRCh38 |
| NC_000001.10:g.207627289G>A , CM000663.1:g.207627289G>A | GRCh37 |
| NC_000001.9:g.205693912G>A | NCBI36 |
| NG_013006.1:g.4645G>A , LRG_348:g.4645G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699640.1:c.-385+849G>A | ENSP00000514493.1:n.-385+849G>A |