Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48523912G>T , CM000685.2:g.48523912G>T | GRCh38 |
| NC_000023.10:g.48382300G>T , CM000685.1:g.48382300G>T | GRCh37 |
| NC_000023.9:g.48267244G>T | NCBI36 |
| NG_007452.1:g.7137G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006579.3:c.141G>T MANE Select | NP_006570.1:p.Trp47Cys |
| ENST00000495186.6:c.141G>T MANE Select | ENSP00000417052.1:p.Trp47Cys |
| NM_006579.2:c.141G>T | NP_006570.1:p.Trp47Cys |
| ENST00000276096.10:n.110-11G>T | |
| ENST00000414061.1:c.141G>T | ENSP00000405832.1:p.Trp47Cys |
| ENST00000446158.5:c.141G>T | ENSP00000390031.1:p.Trp47Cys |
| ENST00000495186.5:c.141G>T | ENSP00000417052.1:p.Trp47Cys |
| ENST00000498425.1:n.262G>T | |
| ENST00000651615.1:c.141G>T | ENSP00000498524.1:p.Trp47Cys |