Linked Data
gnomAD v4:
12-52651914-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52651914C>T , CM000674.2:g.52651914C>T | GRCh38 |
| NC_000012.11:g.53045698C>T , CM000674.1:g.53045698C>T | GRCh37 |
| NC_000012.10:g.51331965C>T | NCBI36 |
| NG_008296.1:g.5262G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309680.4:c.229G>A MANE Select | ENSP00000310861.3:p.Ala77Thr | |
| ENST00000309680.3:c.229G>A | ENSP00000310861.3:p.Ala77Thr | |
| NM_000423.2:c.229G>A | NP_000414.2:p.Ala77Thr | |
| NM_000423.3:c.229G>A MANE Select | NP_000414.2:p.Ala77Thr |