Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924306T>C , CM000675.2:g.27924306T>C | GRCh38 |
| NC_000013.10:g.28498443T>C , CM000675.1:g.28498443T>C | GRCh37 |
| NC_000013.9:g.27396443T>C | NCBI36 |
| NG_008183.1:g.9276T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.457T>C MANE Select | ENSP00000370421.4:p.Tyr153His | |
| ENST00000381033.4:c.457T>C | ENSP00000370421.4:p.Tyr153His | |
| NM_000209.3:c.457T>C | NP_000200.1:p.Tyr153His | |
| XR_941579.1:n.2183T>C | ||
| XR_941580.1:n.1099T>C | ||
| XR_941580.2:n.1111T>C | ||
| NM_000209.4:c.457T>C MANE Select | NP_000200.1:p.Tyr153His |