Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257401T= , CM000671.2:g.133257401T= | GRCh38 |
| NC_000009.11:g.136132788T= , CM000671.1:g.136132788T= | GRCh37 |
| NC_000009.10:g.135122609T= | NCBI36 |
| NG_006669.1:g.20267A= | |
| NG_006669.2:g.22815A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.403+8A= | ||
| ENST00000647353.1:n.54-6249A= | ||
| ENST00000651471.1:n.329+641A= | ||
| ENST00000679909.1:c.28+17761A= | ENSP00000506089.1:n.28+17761A= | |
| ENST00000453660.3:n.385+8A= | ||
| ENST00000538324.2:c.371+8A= | ENSP00000483018.1:n.371+8A= | |
| ENST00000611156.4:c.371+8A= | ENSP00000483265.1:n.371+8A= | |
| NM_020469.2:c.374+8A= | NP_065202.2:n.374+8A= | |
| NM_020469.3:c.374+8A= | NP_065202.2:n.374+8A= |