Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37728007T= , CM000685.2:g.37728007T= | GRCh38 |
| NC_000023.10:g.37587260T= , CM000685.1:g.37587260T= | GRCh37 |
| NC_000023.9:g.37472199T= | NCBI36 |
| NG_007473.1:g.47148T= | |
| NG_007473.3:g.47128T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021083.4:c.880T= MANE Select | NP_066569.1:p.Cys294= |
| ENST00000378616.5:c.880T= MANE Select | ENSP00000367879.3:p.Cys294= |
| NM_021083.2:c.880T= | NP_066569.1:p.Cys294= |
| ENST00000378616.3:c.880T= | ENSP00000367879.3:p.Cys294= |
| ENST00000465127.1:c.171+302007T= | ENSP00000417050.1:n.171+302007T= |