Linked Data
dbSNP Id:
rs1782416904
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151526740del , CM000668.2:g.151526740del | GRCh38 |
| NC_000006.11:g.151847875del , CM000668.1:g.151847875del | GRCh37 |
| NC_000006.10:g.151889568del | NCBI36 |
| NG_021198.1:g.37701del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000239374.8:c.58-9578del MANE Select | ENSP00000239374.6:n.58-9578del | |
| ENST00000239374.7:c.58-9578del | ENSP00000239374.6:n.58-9578del | |
| NM_025059.3:c.58-9578del | NP_079335.2:n.58-9578del | |
| NM_025059.4:c.58-9578del MANE Select | NP_079335.2:n.58-9578del |