Linked Data
dbSNP Id:
rs2084794450
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532861del , CM000665.2:g.129532861del | GRCh38 |
| NC_000003.11:g.129251704del , CM000665.1:g.129251704del | GRCh37 |
| NC_000003.10:g.130734394del | NCBI36 |
| NG_009115.1:g.9223del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.936+89del MANE Select | ENSP00000296271.3:n.936+89del | |
| ENST00000296271.3:c.936+89del | ENSP00000296271.3:n.936+89del | |
| NM_000539.3:c.936+89del MANE Select | NP_000530.1:n.936+89del |