Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49991728G>C , CM000679.2:g.49991728G>C | GRCh38 |
| NC_000017.10:g.48069092G>C , CM000679.1:g.48069092G>C | GRCh37 |
| NC_000017.9:g.45424091G>C | NCBI36 |
| NG_023063.1:g.8497C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000434704.2:c.653C>G MANE Select | ENSP00000389870.2:p.Thr218Ser | |
| ENST00000512495.2:c.293C>G | ENSP00000449976.1:p.Thr98Ser | |
| NM_005220.2:c.653C>G | NP_005211.1:p.Thr218Ser | |
| XM_011524458.1:c.516+1672C>G | XP_011522760.1:n.516+1672C>G | |
| NM_005220.3:c.653C>G MANE Select | NP_005211.1:p.Thr218Ser |