Linked Data
dbSNP Id:
rs1907458117
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584416_41584417insCA , CM000679.2:g.41584416_41584417insCA | GRCh38 |
| NC_000017.10:g.39740668_39740669insCA , CM000679.1:g.39740668_39740669insCA | GRCh37 |
| NC_000017.9:g.36994194_36994195insCA | NCBI36 |
| NG_008624.1:g.7479_7480insTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.609-4_609-3insTG MANE Select | ENSP00000167586.6:n.609-4_609-3insTG | |
| ENST00000167586.6:c.609-4_609-3insTG | ENSP00000167586.6:n.609-4_609-3insTG | |
| ENST00000476662.1:n.55_56insTG | ||
| NM_000526.4:c.609-4_609-3insTG | NP_000517.2:n.609-4_609-3insTG | |
| NM_000526.5:c.609-4_609-3insTG MANE Select | NP_000517.3:n.609-4_609-3insTG |