Linked Data
gnomAD v4:
12-48981745-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981745T>A , CM000674.2:g.48981745T>A | GRCh38 |
| NC_000012.11:g.49375528T>A , CM000674.1:g.49375528T>A | GRCh37 |
| NC_000012.10:g.47661795T>A | NCBI36 |
| NG_033141.1:g.8293T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*105T>A MANE Select | ENSP00000293549.3:n.*105T>A | |
| NM_005430.3:c.*105T>A | NP_005421.1:n.*105T>A | |
| NM_005430.4:c.*105T>A MANE Select | NP_005421.1:n.*105T>A |