Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924266C>G , CM000675.2:g.27924266C>G | GRCh38 |
| NC_000013.10:g.28498403C>G , CM000675.1:g.28498403C>G | GRCh37 |
| NC_000013.9:g.27396403C>G | NCBI36 |
| NG_008183.1:g.9236C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.417C>G MANE Select | ENSP00000370421.4:p.Tyr139Ter | |
| ENST00000381033.4:c.417C>G | ENSP00000370421.4:p.Tyr139Ter | |
| NM_000209.3:c.417C>G | NP_000200.1:p.Tyr139Ter | |
| XR_941578.1:n.3544C>G | ||
| XR_941579.1:n.2143C>G | ||
| XR_941580.1:n.1059C>G | ||
| XR_941578.2:n.3556C>G | ||
| XR_941580.2:n.1071C>G | ||
| NM_000209.4:c.417C>G MANE Select | NP_000200.1:p.Tyr139Ter |