Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.134200572C>A , CM000666.2:g.134200572C>A | GRCh38 |
| NC_000004.11:g.135121727C>A , CM000666.1:g.135121727C>A | GRCh37 |
| NC_000004.10:g.135341177C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000421491.4:c.448G>T MANE Select | ENSP00000463233.1:p.Ala150Ser | |
| ENST00000421491.3:c.448G>T | ENSP00000463233.1:p.Ala150Ser | |
| NM_001114734.1:c.622G>T | NP_001108206.2:p.Ala208Ser | |
| NM_001114734.2:c.448G>T MANE Select | NP_001108206.3:p.Ala150Ser | |
| NM_001363585.1:c.448G>T | NP_001350514.1:p.Ala150Ser | |
| XR_001741133.1:n.987G>T | ||
| XR_001741134.1:n.987G>T | ||
| XR_001741135.1:n.987G>T | ||
| XR_001741136.1:n.987G>T | ||
| XR_001741137.1:n.987G>T | ||
| XR_001741138.1:n.987G>T | ||
| XR_001741139.1:n.982G>T |