Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29065014G>A , CM000664.2:g.29065014G>A | GRCh38 |
| NC_000002.11:g.29287880G>A , CM000664.1:g.29287880G>A | GRCh37 |
| NC_000002.10:g.29141384G>A | NCBI36 |
| NG_021427.1:g.14248C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029883.3:c.3722C>T MANE Select | NP_001025054.1:p.Ser1241Phe |
| ENST00000331664.6:c.3722C>T MANE Select | ENSP00000332809.4:p.Ser1241Phe |
| NM_001029883.2:c.3722C>T | NP_001025054.1:p.Ser1241Phe |
| ENST00000331664.5:c.3722C>T | ENSP00000332809.4:p.Ser1241Phe |
| XM_011532826.1:c.3722C>T | XP_011531128.1:p.Ser1241Phe |
| XR_939901.1:n.69+1119G>A | |
| XR_939902.1:n.69+1119G>A |