Linked Data
dbSNP Id:
rs1031297916
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169586504C>A , CM000663.2:g.169586504C>A | GRCh38 |
| NC_000001.10:g.169555742C>A , CM000663.1:g.169555742C>A | GRCh37 |
| NC_000001.9:g.167822366C>A | NCBI36 |
| NG_011806.1:g.5028G>T , LRG_553:g.5028G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367796.3:c.-118G>T | ENSP00000356770.3:n.-118G>T | |
| ENST00000367797.7:c.-118G>T | ENSP00000356771.3:n.-118G>T | |
| NM_000130.4:c.-118G>T , LRG_553t1:c.-118G>T | NP_000121.2:n.-118G>T | |
| XM_017000660.2:c.-437G>T | XP_016856149.1:n.-437G>T |