Linked Data
dbSNP Id:
rs2103356792
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21010248dup , CM000664.2:g.21010248dup | GRCh38 |
| NC_000002.11:g.21233120dup , CM000664.1:g.21233120dup | GRCh37 |
| NC_000002.10:g.21086625dup | NCBI36 |
| NG_011793.1:g.38830dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.6624dup MANE Select | ENSP00000233242.1:p.Leu2209IlefsTer5 | |
| ENST00000616098.4:c.6624dup | ENSP00000477990.1:p.Leu2209IlefsTer5 | |
| NM_000384.2:c.6624dup | NP_000375.2:p.Leu2209IlefsTer5 | |
| XM_011532809.1:c.5869+489dup | XP_011531111.1:n.5869+489dup | |
| NM_000384.3:c.6624dup MANE Select | NP_000375.3:p.Leu2209IlefsTer5 |