Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955863C>T , CM000670.2:g.19955863C>T | GRCh38 |
| NC_000008.10:g.19813374C>T , CM000670.1:g.19813374C>T | GRCh37 |
| NC_000008.9:g.19857654C>T | NCBI36 |
| NG_008855.1:g.21793C>T | |
| NG_008855.2:g.59147C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.798C>T MANE Select | NP_000228.1:p.Cys266= |
| ENST00000650287.1:c.798C>T MANE Select | ENSP00000497642.1:p.Cys266= |
| NM_000237.2:c.798C>T | NP_000228.1:p.Cys266= |
| ENST00000311322.8:c.798C>T | ENSP00000309757.6:p.Cys266= |