Linked Data
gnomAD v4:
15-42957932-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42957932T>A , CM000677.2:g.42957932T>A | GRCh38 |
| NC_000015.9:g.43250130T>A , CM000677.1:g.43250130T>A | GRCh37 |
| NC_000015.8:g.41037422T>A | NCBI36 |
| NG_012182.1:g.153157A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290650.9:c.4835+81A>T MANE Select | ENSP00000290650.4:n.4835+81A>T | |
| ENST00000290650.8:c.4835+81A>T | ENSP00000290650.4:n.4835+81A>T | |
| NM_174916.2:c.4835+81A>T | NP_777576.1:n.4835+81A>T | |
| NM_174916.3:c.4835+81A>T MANE Select | NP_777576.1:n.4835+81A>T |