Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725612G>C , CM000685.2:g.153725612G>C | GRCh38 |
| NC_000023.10:g.152991067G>C , CM000685.1:g.152991067G>C | GRCh37 |
| NC_000023.9:g.152644261G>C | NCBI36 |
| NG_009022.2:g.5745G>C | |
| NG_023231.1:g.4135C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.346G>C MANE Select | ENSP00000218104.3:p.Gly116Arg | |
| ENST00000218104.5:c.346G>C | ENSP00000218104.3:p.Gly116Arg | |
| NM_000033.3:c.346G>C | NP_000024.2:p.Gly116Arg | |
| XR_938507.1:n.762G>C | ||
| XR_938507.2:n.762G>C | ||
| NM_000033.4:c.346G>C MANE Select | NP_000024.2:p.Gly116Arg |