Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153726105G>C , CM000685.2:g.153726105G>C | GRCh38 |
| NC_000023.10:g.152991560G>C , CM000685.1:g.152991560G>C | GRCh37 |
| NC_000023.9:g.152644754G>C | NCBI36 |
| NG_009022.2:g.6238G>C | |
| NG_023231.1:g.3642C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.839G>C MANE Select | NP_000024.2:p.Arg280Pro |
| ENST00000218104.6:c.839G>C MANE Select | ENSP00000218104.3:p.Arg280Pro |
| NM_000033.3:c.839G>C | NP_000024.2:p.Arg280Pro |
| ENST00000218104.5:c.839G>C | ENSP00000218104.3:p.Arg280Pro |
| ENST00000370129.4:c.284G>C | ENSP00000359147.3:p.Arg95Pro |
| XR_938507.1:n.1255G>C | |
| XR_938507.2:n.1255G>C |