Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942312G= , CM000672.2:g.94942312G= | GRCh38 |
| NC_000010.10:g.96702069G= , CM000672.1:g.96702069G= | GRCh37 |
| NC_000010.9:g.96692059G= | NCBI36 |
| NG_008385.1:g.8655G= | |
| NG_008385.2:g.9155G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.452G= MANE Select | ENSP00000260682.6:p.Cys151= | |
| ENST00000643112.1:c.452G= | ENSP00000496202.1:p.Cys151= | |
| ENST00000645207.1:n.605G= | ||
| ENST00000260682.6:c.452G= | ENSP00000260682.6:p.Cys151= | |
| ENST00000461906.1:n.477G= | ||
| ENST00000473496.1:n.223G= | ||
| NM_000771.3:c.452G= | NP_000762.2:p.Cys151= | |
| NM_000771.4:c.452G= MANE Select | NP_000762.2:p.Cys151= |