Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.43030463A>T , CM000666.2:g.43030463A>T | GRCh38 |
| NC_000004.11:g.43032480A>T , CM000666.1:g.43032480A>T | GRCh37 |
| NC_000004.10:g.42727237A>T | NCBI36 |
| NG_027718.1:g.142198A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080476.3:c.796A>T MANE Select | NP_001073945.1:p.Thr266Ser |
| ENST00000399770.3:c.796A>T MANE Select | ENSP00000382670.2:p.Thr266Ser |
| NM_001080476.2:c.796A>T | NP_001073945.1:p.Thr266Ser |
| ENST00000399770.2:c.796A>T | ENSP00000382670.2:p.Thr266Ser |
| XM_011513691.1:c.433A>T | XP_011511993.1:p.Thr145Ser |