Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.59023552C>T , CM000682.2:g.59023552C>T | GRCh38 |
| NC_000020.10:g.57598607C>T , CM000682.1:g.57598607C>T | GRCh37 |
| NC_000020.9:g.57032002C>T | NCBI36 |
| NG_023424.2:g.9299C>T , LRG_581:g.9299C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_030773.4:c.229C>T MANE Select | NP_110400.1:p.Arg77Ter |
| ENST00000217133.2:c.229C>T MANE Select | ENSP00000217133.1:p.Arg77Ter |
| NM_030773.3:c.229C>T , LRG_581t1:c.229C>T | NP_110400.1:p.Arg77Ter |
| ENST00000217133.1:c.229C>T | ENSP00000217133.1:p.Arg77Ter |
| XM_017028085.1:c.163C>T | XP_016883574.1:p.Arg55Ter |