Linked Data
gnomAD v4:
12-57094633-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57094633A>T , CM000674.2:g.57094633A>T | GRCh38 |
| NC_000012.11:g.57488416A>T , CM000674.1:g.57488416A>T | GRCh37 |
| NC_000012.10:g.55774683A>T | NCBI36 |
| NG_021272.1:g.21781T>A | |
| NG_021272.2:g.42507T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300131.8:c.1490A>T MANE Select | ENSP00000300131.3:p.Asp497Val | |
| ENST00000300131.7:c.1490A>T | ENSP00000300131.3:p.Asp497Val | |
| ENST00000342556.6:c.1298A>T | ENSP00000341491.6:p.Asp433Val | |
| NM_005967.3:c.1490A>T | NP_005958.1:p.Asp497Val | |
| XM_005268894.2:c.1298A>T | XP_005268951.1:p.Asp433Val | |
| NM_001330305.1:c.1298A>T | NP_001317234.1:p.Asp433Val | |
| NM_005967.4:c.1490A>T MANE Select | NP_005958.1:p.Asp497Val | |
| NM_001330305.2:c.1298A>T | NP_001317234.1:p.Asp433Val |