Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131851157G= , CM000668.2:g.131851157G= | GRCh38 |
| NC_000006.11:g.132172297G= , CM000668.1:g.132172297G= | GRCh37 |
| NC_000006.10:g.132213990G= | NCBI36 |
| NG_008206.1:g.48142G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006208.3:c.446G= MANE Select | NP_006199.2:p.Cys149= |
| ENST00000647893.1:c.446G= MANE Select | ENSP00000498074.1:p.Cys149= |
| NM_006208.2:c.446G= | NP_006199.2:p.Cys149= |
| ENST00000360971.6:c.446G= | ENSP00000354238.2:p.Cys149= |
| ENST00000486853.1:n.466G= | |
| ENST00000513998.5:c.446G= | ENSP00000422424.1:p.Cys149= |
| ENST00000650147.1:c.124G= | |
| ENST00000650437.1:c.108+1051G= |