Linked Data
gnomAD v4:
1-192811752-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192811752G>A , CM000663.2:g.192811752G>A | GRCh38 |
| NC_000001.10:g.192780882G>A , CM000663.1:g.192780882G>A | GRCh37 |
| NC_000001.9:g.191047505G>A | NCBI36 |
| NG_012800.1:g.7714G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000235382.7:c.*156G>A MANE Select | ENSP00000235382.5:n.*156G>A | |
| ENST00000235382.6:c.*156G>A | ENSP00000235382.5:n.*156G>A | |
| NM_002923.3:c.*156G>A | NP_002914.1:n.*156G>A | |
| NM_002923.4:c.*156G>A MANE Select | NP_002914.1:n.*156G>A |