Linked Data
dbSNP Id:
rs1938157695
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7086435_7086480del , CM000674.2:g.7086435_7086480del | GRCh38 |
| NG_062465.1:g.11131_11176del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647956.2:c.1039-20_1064del | ||
| ENST00000648162.1:n.1011-20_1036del | ||
| ENST00000649804.1:c.133-20_158del | ||
| ENST00000535233.6:c.937-20_962del | ||
| ENST00000536053.6:c.1081-20_1106del | ||
| ENST00000540394.5:n.2104-20_2129del | ||
| ENST00000542285.5:c.1039-20_1064del | ||
| ENST00000602298.2:n.1368_1413del | ||
| NM_001733.4:c.1039-20_1064del | ||
| NM_001354346.1:c.1081-20_1106del | ||
| NM_001733.6:c.1039-20_1064del | ||
| NM_001733.7:c.1039-20_1064del | ||
| NM_001354346.2:c.1081-20_1106del |