Linked Data
MyVariant Identifiers:
chrX:g.50659226C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50916226C>G , CM000685.2:g.50916226C>G | GRCh38 |
| NC_000023.10:g.50659226C>G , CM000685.1:g.50659226C>G | GRCh37 |
| NC_000023.9:g.50675966C>G | NCBI36 |
| NG_012894.1:g.10443C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.798C>G MANE Select | ENSP00000252677.3:p.Thr266= | |
| ENST00000252677.3:c.798C>G | ENSP00000252677.3:p.Thr266= | |
| NM_005448.2:c.798C>G MANE Select | NP_005439.2:p.Thr266= |