Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110345249_110345250del , CM000674.2:g.110345249_110345250del | GRCh38 |
| NC_000012.11:g.110783054_110783055del , CM000674.1:g.110783054_110783055del | GRCh37 |
| NC_000012.10:g.109267437_109267438del | NCBI36 |
| NG_007097.2:g.68623_68624del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539276.7:c.2608_2609del | ||
| ENST00000308664.10:c.2608_2609del | ||
| ENST00000377685.9:c.*2448_*2449del | ||
| ENST00000539276.6:c.2608_2609del | ||
| ENST00000548169.2:c.2279_2280del | ||
| NM_001681.3:c.2608_2609del | ||
| NM_170665.3:c.2608_2609del | ||
| XM_005253888.1:c.2608_2609del | ||
| XM_011538402.1:c.2608_2609del | ||
| XR_243009.1:n.2614_2615del | ||
| XM_005253888.3:c.2608_2609del | ||
| XM_011538402.3:c.2608_2609del | ||
| XR_002957329.1:n.2614_2615del | ||
| XR_243009.3:n.2614_2615del | ||
| NM_170665.4:c.2608_2609del | ||
| NM_001681.4:c.2608_2609del |