Linked Data
gnomAD v4:
12-48981806-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981806T>A , CM000674.2:g.48981806T>A | GRCh38 |
| NC_000012.11:g.49375589T>A , CM000674.1:g.49375589T>A | GRCh37 |
| NC_000012.10:g.47661856T>A | NCBI36 |
| NG_033141.1:g.8354T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*166T>A MANE Select | ENSP00000293549.3:n.*166T>A | |
| NM_005430.3:c.*166T>A | NP_005421.1:n.*166T>A | |
| NM_005430.4:c.*166T>A MANE Select | NP_005421.1:n.*166T>A |