Linked Data
gnomAD v4:
X-153726142-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153726142G>T , CM000685.2:g.153726142G>T | GRCh38 |
| NC_000023.10:g.152991597G>T , CM000685.1:g.152991597G>T | GRCh37 |
| NC_000023.9:g.152644791G>T | NCBI36 |
| NG_009022.2:g.6275G>T | |
| NG_023231.1:g.3605C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.876G>T MANE Select | ENSP00000218104.3:p.Glu292Asp | |
| ENST00000218104.5:c.876G>T | ENSP00000218104.3:p.Glu292Asp | |
| ENST00000370129.4:c.321G>T | ENSP00000359147.3:p.Glu107Asp | |
| NM_000033.3:c.876G>T | NP_000024.2:p.Glu292Asp | |
| XR_938507.1:n.1292G>T | ||
| XR_938507.2:n.1292G>T | ||
| NM_000033.4:c.876G>T MANE Select | NP_000024.2:p.Glu292Asp |