Linked Data
dbSNP Id:
rs2084771005
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129530528_129530529insGCA , CM000665.2:g.129530528_129530529insGCA | GRCh38 |
| NC_000003.11:g.129249371_129249372insGCA , CM000665.1:g.129249371_129249372insGCA | GRCh37 |
| NC_000003.10:g.130732061_130732062insGCA | NCBI36 |
| NG_009115.1:g.6890_6891insGCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.362-348_362-347insGCA MANE Select | ENSP00000296271.3:n.362-348_362-347insGCA | |
| ENST00000296271.3:c.362-348_362-347insGCA | ENSP00000296271.3:n.362-348_362-347insGCA | |
| NM_000539.3:c.362-348_362-347insGCA MANE Select | NP_000530.1:n.362-348_362-347insGCA |