Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924615G>T , CM000675.2:g.27924615G>T | GRCh38 |
| NC_000013.10:g.28498752G>T , CM000675.1:g.28498752G>T | GRCh37 |
| NC_000013.9:g.27396752G>T | NCBI36 |
| NG_008183.1:g.9585G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.766G>T MANE Select | ENSP00000370421.4:p.Ala256Ser | |
| ENST00000381033.4:c.766G>T | ENSP00000370421.4:p.Ala256Ser | |
| NM_000209.3:c.766G>T | NP_000200.1:p.Ala256Ser | |
| NM_000209.4:c.766G>T MANE Select | NP_000200.1:p.Ala256Ser |