Linked Data
dbSNP Id:
rs1762508087
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610153_1610154insTT , CM000668.2:g.1610153_1610154insTT | GRCh38 |
| NC_000006.11:g.1610388_1610389insTT , CM000668.1:g.1610388_1610389insTT | GRCh37 |
| NC_000006.10:g.1555387_1555388insTT | NCBI36 |
| NG_009368.1:g.4708_4709insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.-293_-292insTT MANE Select | ENSP00000493906.1:n.-293_-292insTT | |
| ENST00000380874.3:c.-293_-292insTT | ENSP00000370256.2:n.-293_-292insTT | |
| NM_001453.3:c.-293_-292insTT MANE Select | NP_001444.2:n.-293_-292insTT |