Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256326C= , CM000671.2:g.133256326C= | GRCh38 |
| NC_000009.11:g.136131713C= , CM000671.1:g.136131713C= | GRCh37 |
| NC_000009.10:g.135121534C= | NCBI36 |
| NG_006669.1:g.21342G= | |
| NG_006669.2:g.23890G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.434G= | ||
| ENST00000647353.1:n.54-5174G= | ||
| ENST00000651471.1:n.360G= | ||
| ENST00000679909.1:c.28+18836G= | ENSP00000506089.1:n.28+18836G= | |
| ENST00000453660.3:n.416G= | ||
| ENST00000538324.2:c.402G= | ENSP00000483018.1:p.Glu134= | |
| ENST00000611156.4:c.402G= | ENSP00000483265.1:p.Glu134= | |
| NM_020469.2:c.405G= | NP_065202.2:p.Glu135= | |
| NM_020469.3:c.405G= | NP_065202.2:p.Glu135= |