Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47332648C>G , CM000673.2:g.47332648C>G | GRCh38 |
| NC_000011.9:g.47354199C>G , CM000673.1:g.47354199C>G | GRCh37 |
| NC_000011.8:g.47310775C>G | NCBI36 |
| NG_007667.1:g.25055G>C , LRG_386:g.25055G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.3545G>C MANE Select | ENSP00000442795.1:p.Ser1182Thr | |
| ENST00000256993.8:c.3545G>C | ENSP00000256993.5:p.Ser1182Thr | |
| ENST00000399249.6:c.3545G>C | ENSP00000382193.2:p.Ser1182Thr | |
| ENST00000545968.5:c.3545G>C | ENSP00000442795.1:p.Ser1182Thr | |
| NM_000256.3:c.3545G>C , LRG_386t1:c.3545G>C MANE Select | NP_000247.2:p.Ser1182Thr | |
| XM_011520117.1:c.3527G>C | XP_011518419.1:p.Ser1176Thr | |
| XM_011520118.1:c.3464G>C | XP_011518420.1:p.Ser1155Thr |