Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65029552C>G , CM000677.2:g.65029552C>G | GRCh38 |
| NC_000015.9:g.65321890C>G , CM000677.1:g.65321890C>G | GRCh37 |
| NC_000015.8:g.63108943C>G | NCBI36 |
| NG_029184.1:g.5088G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220058.9:c.62G>C MANE Select | ENSP00000220058.4:p.Arg21Thr | |
| ENST00000220058.8:c.62G>C | ENSP00000220058.4:p.Arg21Thr | |
| ENST00000543678.1:c.62G>C | ENSP00000443754.1:p.Arg21Thr | |
| ENST00000558460.5:c.62G>C | ENSP00000452646.1:p.Arg21Thr | |
| ENST00000558614.1:n.23G>C | ||
| ENST00000560717.5:c.47G>C | ENSP00000457257.1:p.Arg16Thr | |
| NM_139242.3:c.62G>C | NP_640335.2:p.Arg21Thr | |
| XM_005254158.5:c.62G>C | XP_005254215.2:p.Arg21Thr | |
| XR_001751081.1:n.77G>C | ||
| NM_139242.4:c.62G>C MANE Select | NP_640335.2:p.Arg21Thr |