Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56042463C>T , CM000674.2:g.56042463C>T | GRCh38 |
| NC_000012.11:g.56436247C>T , CM000674.1:g.56436247C>T | GRCh37 |
| NC_000012.10:g.54722514C>T | NCBI36 |
| NG_023201.1:g.5562C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029.5:c.42C>T MANE Select | NP_001020.2:p.Gly14= |
| ENST00000646449.2:c.42C>T MANE Select | ENSP00000496643.1:p.Gly14= |
| NM_001029.3:c.42C>T | NP_001020.2:p.Gly14= |
| ENST00000356464.10:c.42C>T | ENSP00000348849.5:p.Gly14= |
| ENST00000356464.9:c.42C>T | ENSP00000348849.5:p.Gly14= |
| ENST00000548590.1:n.69C>T | |
| ENST00000552361.1:c.42C>T | ENSP00000450339.1:p.Gly14= |