Linked Data
gnomAD v4:
1-207454252-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207454252A>T , CM000663.2:g.207454252A>T | GRCh38 |
| NC_000001.10:g.207627597A>T , CM000663.1:g.207627597A>T | GRCh37 |
| NC_000001.9:g.205694220A>T | NCBI36 |
| NG_013006.1:g.4953A>T , LRG_348:g.4953A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000699640.1:c.-385+1157A>T | ENSP00000514493.1:n.-385+1157A>T | |
| ENST00000367057.7:c.-167A>T | ENSP00000356024.3:n.-167A>T | |
| ENST00000367058.7:c.-167A>T | ENSP00000356025.3:n.-167A>T | |
| ENST00000367059.3:c.-167A>T | ENSP00000356026.3:n.-167A>T |