Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257426A= , CM000671.2:g.133257426A= | GRCh38 |
| NC_000009.11:g.136132813A= , CM000671.1:g.136132813A= | GRCh37 |
| NC_000009.10:g.135122634A= | NCBI36 |
| NG_006669.1:g.20242T= | |
| NG_006669.2:g.22790T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.386T= | ||
| ENST00000647353.1:n.54-6274T= | ||
| ENST00000651471.1:n.329+616T= | ||
| ENST00000679909.1:c.28+17736T= | ENSP00000506089.1:n.28+17736T= | |
| ENST00000453660.3:n.368T= | ||
| ENST00000538324.2:c.354T= | ENSP00000483018.1:p.Thr118= | |
| ENST00000611156.4:c.354T= | ENSP00000483265.1:p.Thr118= | |
| NM_020469.2:c.357T= | NP_065202.2:p.Thr119= | |
| NM_020469.3:c.357T= | NP_065202.2:p.Thr119= |