Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40472135C>T , CM000677.2:g.40472135C>T | GRCh38 |
| NC_000015.9:g.40764334C>T , CM000677.1:g.40764334C>T | GRCh37 |
| NC_000015.8:g.38551626C>T | NCBI36 |
| NG_017074.1:g.6175C>T , LRG_600:g.6175C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_130468.4:c.922C>T MANE Select | NP_569735.1:p.Gln308Ter |
| ENST00000306243.7:c.922C>T MANE Select | ENSP00000307297.6:p.Gln308Ter |
| NM_130468.3:c.922C>T , LRG_600t1:c.922C>T | NP_569735.1:p.Gln308Ter |
| ENST00000306243.6:c.922C>T | ENSP00000307297.5:p.Gln308Ter |
| ENST00000559991.1:c.847C>T | ENSP00000453882.1:p.Gln283Ter |