Linked Data
gnomAD v4:
1-169586585-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169586585T>C , CM000663.2:g.169586585T>C | GRCh38 |
| NC_000001.10:g.169555823T>C , CM000663.1:g.169555823T>C | GRCh37 |
| NC_000001.9:g.167822447T>C | NCBI36 |
| NG_011806.1:g.4947A>G , LRG_553:g.4947A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367796.3:c.-199A>G | ENSP00000356770.3:n.-199A>G | |
| ENST00000367797.7:c.-199A>G | ENSP00000356771.3:n.-199A>G | |
| XM_017000660.2:c.-518A>G | XP_016856149.1:n.-518A>G |