Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257328T= , CM000671.2:g.133257328T= | GRCh38 |
| NC_000009.11:g.136132715T= , CM000671.1:g.136132715T= | GRCh37 |
| NC_000009.10:g.135122536T= | NCBI36 |
| NG_006669.1:g.20340A= | |
| NG_006669.2:g.22888A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.403+81A= | ||
| ENST00000647353.1:n.54-6176A= | ||
| ENST00000651471.1:n.329+714A= | ||
| ENST00000679909.1:c.28+17834A= | ENSP00000506089.1:n.28+17834A= | |
| ENST00000453660.3:n.385+81A= | ||
| ENST00000538324.2:c.371+81A= | ENSP00000483018.1:n.371+81A= | |
| ENST00000611156.4:c.371+81A= | ENSP00000483265.1:n.371+81A= | |
| NM_020469.2:c.374+81A= | NP_065202.2:n.374+81A= | |
| NM_020469.3:c.374+81A= | NP_065202.2:n.374+81A= |