Linked Data
dbSNP Id:
rs1732600117
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.156971731del , CM000666.2:g.156971731del | GRCh38 |
| NC_000004.11:g.157892883del , CM000666.1:g.157892883del | GRCh37 |
| NC_000004.10:g.158112333del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502773.6:c.-825del MANE Select | ENSP00000422464.1:n.-825del | |
| NM_016205.3:c.-825del MANE Select | NP_057289.1:n.-825del | |
| NR_036641.2:n.72del |