Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119335886C>G , CM000673.2:g.119335886C>G | GRCh38 |
| NC_000011.9:g.119206596C>G , CM000673.1:g.119206596C>G | GRCh37 |
| NC_000011.8:g.118711806C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311413.5:c.764C>G MANE Select | ENSP00000312439.4:p.Thr255Ser | |
| ENST00000311413.4:c.764C>G | ENSP00000312439.4:p.Thr255Ser | |
| NM_032015.4:c.764C>G | NP_114404.1:p.Thr255Ser | |
| NM_032015.5:c.764C>G MANE Select | NP_114404.1:p.Thr255Ser |