Linked Data
dbSNP Id:
rs1853251302
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.20638458_20638469del , CM000673.2:g.20638458_20638469del | GRCh38 |
| NC_000011.9:g.20660004_20660015del , CM000673.1:g.20660004_20660015del | GRCh37 |
| NC_000011.8:g.20616580_20616591del | NCBI36 |
| NG_013086.1:g.44059_44070del | |
| NG_013086.2:g.44059_44070del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525748.6:c.1870-1_1880del | ||
| ENST00000298923.11:c.*1167-1_*1177del | ||
| ENST00000525748.5:c.1870-1_1880del | ||
| ENST00000528440.1:n.401-1_411del | ||
| NM_004211.3:c.1870-1_1880del | ||
| XM_005253225.1:c.1168-1_1178del | ||
| XM_011520473.1:c.1870-1_1880del | ||
| NM_001318369.1:c.1168-1_1178del | ||
| NM_004211.4:c.1870-1_1880del | ||
| XM_017018544.2:c.994-1_1004del | ||
| XM_017018545.2:c.829-1_839del | ||
| NM_001318369.2:c.1168-1_1178del | ||
| NM_004211.5:c.1870-1_1880del |