Linked Data
dbSNP Id:
rs1755656437
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320835_119320836insG , CM000666.2:g.119320835_119320836insG | GRCh38 |
| NC_000004.11:g.120241990_120241991insG , CM000666.1:g.120241990_120241991insG | GRCh37 |
| NC_000004.10:g.120461438_120461439insG | NCBI36 |
| NG_011444.1:g.6326_6327insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274024.4:c.74_75insC MANE Select | ENSP00000274024.3:p.Ile26TyrfsTer10 | |
| ENST00000274024.3:c.74_75insC | ENSP00000274024.3:p.Ile26TyrfsTer10 | |
| NM_000134.3:c.74_75insC | NP_000125.2:p.Ile26TyrfsTer10 | |
| NM_000134.4:c.74_75insC MANE Select | NP_000125.2:p.Ile26TyrfsTer10 |