Linked Data
gnomAD v4:
X-74421779-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74421779C>A , CM000685.2:g.74421779C>A | GRCh38 |
| NC_000023.10:g.73641614C>A , CM000685.1:g.73641614C>A | GRCh37 |
| NC_000023.9:g.73558339C>A | NCBI36 |
| NG_011641.1:g.5530C>A | |
| NG_011641.2:g.5530C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000587091.6:c.142C>A MANE Select | ENSP00000465734.1:p.Pro48Thr | |
| ENST00000587091.5:c.142C>A | ENSP00000465734.1:p.Pro48Thr | |
| NM_006517.4:c.142C>A | NP_006508.2:p.Pro48Thr | |
| XM_005262294.1:c.142C>A | XP_005262351.1:p.Pro48Thr | |
| XM_011531015.1:c.142C>A | XP_011529317.1:p.Pro48Thr | |
| NM_006517.5:c.142C>A MANE Select | NP_006508.2:p.Pro48Thr |