Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.22786790C>G , CM000677.2:g.22786790C>G | GRCh38 |
| NC_000015.9:g.23086278G>C , CM000677.1:g.23086278G>C | GRCh37 |
| NC_000015.8:g.20637719G>C | NCBI36 |
| NG_009056.1:g.5566C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000337435.9:c.134C>G MANE Select | ENSP00000337452.4:p.Thr45Arg | |
| ENST00000337435.8:c.134C>G | ENSP00000337452.4:p.Thr45Arg | |
| ENST00000437912.6:c.-48+12477C>G | ENSP00000393962.2:n.-48+12477C>G | |
| ENST00000559448.5:c.24C>G | ||
| ENST00000560069.5:n.31+542C>G | ||
| ENST00000560105.1:n.33C>G | ||
| ENST00000561183.5:c.-48+542C>G | ENSP00000453722.1:n.-48+542C>G | |
| NM_001142275.1:c.-48+542C>G | NP_001135747.1:n.-48+542C>G | |
| NM_144599.4:c.134C>G | NP_653200.2:p.Thr45Arg | |
| NM_144599.5:c.134C>G MANE Select | NP_653200.2:p.Thr45Arg |