Linked Data
dbSNP Id:
rs560760659
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583201_41583202insA , CM000679.2:g.41583201_41583202insA | GRCh38 |
| NC_000017.10:g.39739453_39739454insA , CM000679.1:g.39739453_39739454insA | GRCh37 |
| NC_000017.9:g.36992979_36992980insA | NCBI36 |
| NG_008624.1:g.8694_8695insT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000167586.7:c.1274+33_1274+34insT MANE Select | ENSP00000167586.6:n.1274+33_1274+34insT | |
| ENST00000167586.6:c.1274+33_1274+34insT | ENSP00000167586.6:n.1274+33_1274+34insT | |
| ENST00000441550.2:n.221+33_221+34insT | ||
| NM_000526.4:c.1274+33_1274+34insT | NP_000517.2:n.1274+33_1274+34insT | |
| NM_000526.5:c.1274+33_1274+34insT MANE Select | NP_000517.3:n.1274+33_1274+34insT |