Linked Data
MyVariant Identifiers:
chr10:g.124268198T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122508682T>A , CM000672.2:g.122508682T>A | GRCh38 |
| NC_000010.10:g.124268198T>A , CM000672.1:g.124268198T>A | GRCh37 |
| NC_000010.9:g.124258188T>A | NCBI36 |
| NG_011554.1:g.52158T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.1032T>A MANE Select | ENSP00000357980.3:p.Thr344= | |
| ENST00000648167.1:c.714T>A | ENSP00000498033.1:p.Thr238= | |
| ENST00000368984.7:c.1032T>A | ENSP00000357980.3:p.Thr344= | |
| ENST00000420892.1:c.255T>A | ENSP00000412676.1:p.Thr85= | |
| NM_002775.4:c.1032T>A | NP_002766.1:p.Thr344= | |
| NM_002775.5:c.1032T>A MANE Select | NP_002766.1:p.Thr344= |