Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94046961G>C , CM000663.2:g.94046961G>C | GRCh38 |
| NC_000001.10:g.94512517G>C , CM000663.1:g.94512517G>C | GRCh37 |
| NC_000001.9:g.94285105G>C | NCBI36 |
| NG_009073.1:g.79189C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.2876C>G MANE Select | NP_000341.2:p.Thr959Ser |
| ENST00000370225.4:c.2876C>G MANE Select | ENSP00000359245.3:p.Thr959Ser |
| NM_000350.2:c.2876C>G | NP_000341.2:p.Thr959Ser |
| ENST00000370225.3:c.2876C>G | ENSP00000359245.3:p.Thr959Ser |
| ENST00000536513.5:c.-64-6872C>G | ENSP00000439707.2:n.-64-6872C>G |
| ENST00000649773.1:c.2654C>G | ENSP00000496882.1:p.Thr885Ser |