Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45111775C>T , CM000677.2:g.45111775C>T | GRCh38 |
| NC_000015.9:g.45403973C>T , CM000677.1:g.45403973C>T | GRCh37 |
| NC_000015.8:g.43191265C>T | NCBI36 |
| NG_009447.1:g.7387G>A | |
| NG_016992.1:g.2451C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001363711.2:c.506G>A MANE Select | NP_001350640.1:p.Arg169Gln |
| ENST00000389039.11:c.506G>A MANE Select | ENSP00000373691.7:p.Arg169Gln |
| NM_001363711.1:c.506G>A | NP_001350640.1:p.Arg169Gln |
| NM_014080.4:c.506G>A | NP_054799.4:p.Arg169Gln |
| NM_014080.5:c.506G>A | NP_054799.4:p.Arg169Gln |
| ENST00000389039.10:c.506G>A | ENSP00000373691.6:p.Arg169Gln |
| ENST00000558383.1:n.549G>A | |
| ENST00000603300.1:c.506G>A | ENSP00000475084.1:p.Arg169Gln |
| XM_005254421.2:c.506G>A | XP_005254478.1:p.Arg169Gln |