Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542027G>C , CM000671.2:g.98542027G>C | GRCh38 |
| NC_000009.11:g.101304309G>C , CM000671.1:g.101304309G>C | GRCh37 |
| NC_000009.10:g.100344130G>C | NCBI36 |
| NG_016426.1:g.172171C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.476C>G MANE Select | ENSP00000259455.2:p.Thr159Ser | |
| ENST00000637410.1:n.254C>G | ||
| ENST00000637717.1:c.92C>G | ENSP00000490789.1:p.Thr31Ser | |
| ENST00000638001.1:n.86C>G | ||
| ENST00000259455.3:c.476C>G | ENSP00000259455.2:p.Thr159Ser | |
| ENST00000477471.1:n.263C>G | ||
| ENST00000634227.1:n.250C>G | ||
| NM_005458.7:c.476C>G | NP_005449.5:p.Thr159Ser | |
| XM_017015331.2:c.182C>G | XP_016870820.1:p.Thr61Ser | |
| NM_005458.8:c.476C>G MANE Select | NP_005449.5:p.Thr159Ser |