Linked Data
dbSNP Id:
rs1895417645
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.89568631dup , CM000676.2:g.89568631dup | GRCh38 |
| NC_000014.8:g.90034975dup , CM000676.1:g.90034975dup | GRCh37 |
| NC_000014.7:g.89104728dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345097.8:c.-15+50398dup | ENSP00000343288.4:n.-15+50398dup | |
| ENST00000555353.5:c.-15+50398dup | ENSP00000452227.1:n.-15+50398dup | |
| ENST00000555855.5:c.-118+50398dup | ENSP00000451135.1:n.-118+50398dup | |
| NM_001085471.1:c.-15+50398dup | NP_001078940.1:n.-15+50398dup | |
| NM_001085471.2:c.-15+50398dup | NP_001078940.1:n.-15+50398dup |