Linked Data
dbSNP Id:
rs1880068056
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91107239_91107245del , CM000674.2:g.91107239_91107245del | GRCh38 |
| NC_000012.11:g.91501016_91501022del , CM000674.1:g.91501016_91501022del | GRCh37 |
| NC_000012.10:g.90025147_90025153del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266718.5:c.862+873_862+879del MANE Select | ENSP00000266718.4:n.862+873_862+879del | |
| ENST00000266718.4:c.862+873_862+879del | ENSP00000266718.4:n.862+873_862+879del | |
| ENST00000546642.1:n.612+873_612+879del | ||
| ENST00000548071.1:n.255+873_255+879del | ||
| NM_002345.3:c.862+873_862+879del | NP_002336.1:n.862+873_862+879del | |
| NM_002345.4:c.862+873_862+879del MANE Select | NP_002336.1:n.862+873_862+879del |