Linked Data
dbSNP Id:
rs2108749092
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129528703del , CM000665.2:g.129528703del | GRCh38 |
| NC_000003.11:g.129247546del , CM000665.1:g.129247546del | GRCh37 |
| NC_000003.10:g.130730236del | NCBI36 |
| NG_009115.1:g.5065del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.-31del MANE Select | ENSP00000296271.3:n.-31del | |
| ENST00000296271.3:c.-31del | ENSP00000296271.3:n.-31del | |
| NM_000539.3:c.-31del MANE Select | NP_000530.1:n.-31del |