Linked Data
gnomAD v4:
22-50221291-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50221291T>A , CM000684.2:g.50221291T>A | GRCh38 |
| NC_000022.10:g.50659720T>A , CM000684.1:g.50659720T>A | GRCh37 |
| NC_000022.9:g.49001847T>A | NCBI36 |
| NG_032160.1:g.28681A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3068A>T MANE Select | ENSP00000248846.5:p.Glu1023Val | |
| ENST00000248846.9:c.3068A>T | ENSP00000248846.5:p.Glu1023Val | |
| ENST00000439308.6:c.3068A>T | ENSP00000397387.2:p.Glu1023Val | |
| ENST00000491449.5:n.1375A>T | ||
| ENST00000498611.5:n.3601A>T | ||
| NM_020461.3:c.3068A>T | NP_065194.2:p.Glu1023Val | |
| XR_938347.1:n.3633A>T | ||
| XR_938348.1:n.3049+737A>T | ||
| XR_001755343.2:n.3637A>T | ||
| XR_001755344.2:n.3637A>T | ||
| XR_002958720.1:n.3053+737A>T | ||
| XR_938347.2:n.3637A>T | ||
| NM_020461.4:c.3068A>T MANE Select | NP_065194.3:p.Glu1023Val |