Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.24084143T= , CM000675.2:g.24084143T= | GRCh38 |
| NC_000013.10:g.24658282T= , CM000675.1:g.24658282T= | GRCh37 |
| NC_000013.9:g.23556282T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382141.4:c.-112+66442T= | ENSP00000371576.4:n.-112+66442T= | |
| ENST00000424834.6:c.-112+66442T= | ENSP00000398560.2:n.-112+66442T= | |
| NM_001286792.1:c.75+66442T= | NP_001273721.1:n.75+66442T= | |
| NM_001286792.2:c.75+66442T= | NP_001273721.1:n.75+66442T= |