Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153740185G>A , CM000685.2:g.153740185G>A | GRCh38 |
| NC_000023.10:g.153005639G>A , CM000685.1:g.153005639G>A | GRCh37 |
| NC_000023.9:g.152658833G>A | NCBI36 |
| NG_009022.2:g.20318G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.1582G>A MANE Select | NP_000024.2:p.Gly528Ser |
| ENST00000218104.6:c.1582G>A MANE Select | ENSP00000218104.3:p.Gly528Ser |
| NM_000033.3:c.1582G>A | NP_000024.2:p.Gly528Ser |
| ENST00000218104.5:c.1582G>A | ENSP00000218104.3:p.Gly528Ser |
| ENST00000443684.2:n.585G>A | |
| XR_938507.1:n.2054G>A | |
| XR_938507.2:n.2054G>A |