Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56042484T>A , CM000674.2:g.56042484T>A | GRCh38 |
| NC_000012.11:g.56436268T>A , CM000674.1:g.56436268T>A | GRCh37 |
| NC_000012.10:g.54722535T>A | NCBI36 |
| NG_023201.1:g.5583T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.63T>A | ENSP00000348849.5:p.Ile21= | |
| ENST00000646449.2:c.63T>A MANE Select | ENSP00000496643.1:p.Ile21= | |
| ENST00000356464.9:c.63T>A | ENSP00000348849.5:p.Ile21= | |
| ENST00000548590.1:n.90T>A | ||
| ENST00000552361.1:c.63T>A | ENSP00000450339.1:p.Ile21= | |
| NM_001029.3:c.63T>A | NP_001020.2:p.Ile21= | |
| NM_001029.5:c.63T>A MANE Select | NP_001020.2:p.Ile21= |