Linked Data
gnomAD v4:
19-55154092-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154092C>T , CM000681.2:g.55154092C>T | GRCh38 |
| NC_000019.9:g.55665460C>T , CM000681.1:g.55665460C>T | GRCh37 |
| NC_000019.8:g.60357272C>T | NCBI36 |
| NG_007866.2:g.8641G>A , LRG_432:g.8641G>A | |
| NG_011829.2:g.147G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.487G>A MANE Select | ENSP00000341838.5:p.Ala163Thr | |
| ENST00000665070.1:c.520G>A | ENSP00000499482.1:p.Ala174Thr | |
| ENST00000344887.9:c.487G>A | ENSP00000341838.5:p.Ala163Thr | |
| ENST00000585806.5:n.486G>A | ||
| ENST00000588882.1:c.412G>A | ENSP00000466729.1:p.Ala138Thr | |
| ENST00000589864.1:n.315G>A | ||
| NM_000363.4:c.487G>A , LRG_432t1:c.487G>A | NP_000354.4:p.Ala163Thr | |
| NM_000363.5:c.487G>A MANE Select | NP_000354.4:p.Ala163Thr |