Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102867307T>A , CM000673.2:g.102867307T>A | GRCh38 |
| NC_000011.9:g.102738038T>A , CM000673.1:g.102738038T>A | GRCh37 |
| NC_000011.8:g.102243248T>A | NCBI36 |
| NG_032936.1:g.12728A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000571244.3:c.874A>T MANE Select | ENSP00000458585.1:p.Thr292Ser | |
| ENST00000571244.2:c.874A>T | ENSP00000458585.1:p.Thr292Ser | |
| NM_002426.4:c.874A>T | NP_002417.2:p.Thr292Ser | |
| NM_002426.5:c.874A>T | NP_002417.2:p.Thr292Ser | |
| NM_002426.6:c.874A>T MANE Select | NP_002417.2:p.Thr292Ser |