Linked Data
gnomAD v4:
4-68646948-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68646948A>T , CM000666.2:g.68646948A>T | GRCh38 |
| NC_000004.11:g.69512666A>T , CM000666.1:g.69512666A>T | GRCh37 |
| NC_000004.10:g.69195261A>T | NCBI36 |
| NG_052676.1:g.28829T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.*156T>A MANE Select | ENSP00000341045.5:n.*156T>A | |
| ENST00000338206.5:c.*156T>A | ENSP00000341045.5:n.*156T>A | |
| ENST00000616841.4:c.1732+17T>A | ENSP00000482004.1:n.1732+17T>A | |
| NM_001076.3:c.*156T>A | NP_001067.2:n.*156T>A | |
| NM_001076.4:c.*156T>A MANE Select | NP_001067.2:n.*156T>A |