Linked Data
gnomAD v4:
X-21845301-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.21845301T>A , CM000685.2:g.21845301T>A | GRCh38 |
| NC_000023.10:g.21863419T>A , CM000685.1:g.21863419T>A | GRCh37 |
| NC_000023.9:g.21773340T>A | NCBI36 |
| NG_012797.1:g.10764T>A | |
| NG_012797.2:g.10764T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379484.10:c.355T>A MANE Select | ENSP00000368798.5:p.Ser119Thr | |
| ENST00000365779.2:c.355T>A | ENSP00000368796.1:p.Ser119Thr | |
| ENST00000379484.9:c.355T>A | ENSP00000368798.5:p.Ser119Thr | |
| ENST00000465888.1:n.454T>A | ||
| NM_015884.3:c.355T>A | NP_056968.1:p.Ser119Thr | |
| NM_015884.4:c.355T>A MANE Select | NP_056968.1:p.Ser119Thr |