Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725575C>G , CM000685.2:g.153725575C>G | GRCh38 |
| NC_000023.10:g.152991030C>G , CM000685.1:g.152991030C>G | GRCh37 |
| NC_000023.9:g.152644224C>G | NCBI36 |
| NG_009022.2:g.5708C>G | |
| NG_023231.1:g.4172G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.309C>G MANE Select | NP_000024.2:p.Ser103Arg |
| ENST00000218104.6:c.309C>G MANE Select | ENSP00000218104.3:p.Ser103Arg |
| NM_000033.3:c.309C>G | NP_000024.2:p.Ser103Arg |
| ENST00000218104.5:c.309C>G | ENSP00000218104.3:p.Ser103Arg |
| XR_938507.1:n.725C>G | |
| XR_938507.2:n.725C>G |