Linked Data
dbSNP Id:
rs1907438913
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584058_41584059insTT , CM000679.2:g.41584058_41584059insTT | GRCh38 |
| NC_000017.10:g.39740310_39740311insTT , CM000679.1:g.39740310_39740311insTT | GRCh37 |
| NC_000017.9:g.36993836_36993837insTT | NCBI36 |
| NG_008624.1:g.7838_7839insAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-137_766-136insAA MANE Select | ENSP00000167586.6:n.766-137_766-136insAA | |
| ENST00000167586.6:c.766-137_766-136insAA | ENSP00000167586.6:n.766-137_766-136insAA | |
| ENST00000476662.1:n.216-137_216-136insAA | ||
| NM_000526.4:c.766-137_766-136insAA | NP_000517.2:n.766-137_766-136insAA | |
| NM_000526.5:c.766-137_766-136insAA MANE Select | NP_000517.3:n.766-137_766-136insAA |