Linked Data
gnomAD v4:
10-133373278-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133373278A>T , CM000672.2:g.133373278A>T | GRCh38 |
| NC_000010.10:g.135186782A>T , CM000672.1:g.135186782A>T | GRCh37 |
| NC_000010.9:g.135036772A>T | NCBI36 |
| NG_042077.1:g.5127T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.56T>A MANE Select | ENSP00000357535.3:p.Val19Asp | |
| ENST00000368547.3:c.56T>A | ENSP00000357535.3:p.Val19Asp | |
| NM_004092.3:c.56T>A | NP_004083.3:p.Val19Asp | |
| XR_002956965.1:n.119T>A | ||
| NM_004092.4:c.56T>A MANE Select | NP_004083.3:p.Val19Asp |