Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153726153A>C , CM000685.2:g.153726153A>C | GRCh38 |
| NC_000023.10:g.152991608A>C , CM000685.1:g.152991608A>C | GRCh37 |
| NC_000023.9:g.152644802A>C | NCBI36 |
| NG_009022.2:g.6286A>C | |
| NG_023231.1:g.3594T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.887A>C MANE Select | NP_000024.2:p.Tyr296Ser |
| ENST00000218104.6:c.887A>C MANE Select | ENSP00000218104.3:p.Tyr296Ser |
| NM_000033.3:c.887A>C | NP_000024.2:p.Tyr296Ser |
| ENST00000218104.5:c.887A>C | ENSP00000218104.3:p.Tyr296Ser |
| ENST00000370129.4:c.332A>C | ENSP00000359147.3:p.Tyr111Ser |
| XR_938507.1:n.1303A>C | |
| XR_938507.2:n.1303A>C |