Linked Data
gnomAD v4:
1-169586504-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169586504C>T , CM000663.2:g.169586504C>T | GRCh38 |
| NC_000001.10:g.169555742C>T , CM000663.1:g.169555742C>T | GRCh37 |
| NC_000001.9:g.167822366C>T | NCBI36 |
| NG_011806.1:g.5028G>A , LRG_553:g.5028G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367796.3:c.-118G>A | ENSP00000356770.3:n.-118G>A | |
| ENST00000367797.7:c.-118G>A | ENSP00000356771.3:n.-118G>A | |
| NM_000130.4:c.-118G>A , LRG_553t1:c.-118G>A | NP_000121.2:n.-118G>A | |
| XM_017000660.2:c.-437G>A | XP_016856149.1:n.-437G>A |