Linked Data
dbSNP Id:
rs1907432905
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583992del , CM000679.2:g.41583992del | GRCh38 |
| NC_000017.10:g.39740244del , CM000679.1:g.39740244del | GRCh37 |
| NC_000017.9:g.36993770del | NCBI36 |
| NG_008624.1:g.7905del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-70del MANE Select | ENSP00000167586.6:n.766-70del | |
| ENST00000167586.6:c.766-70del | ENSP00000167586.6:n.766-70del | |
| ENST00000476662.1:n.216-70del | ||
| NM_000526.4:c.766-70del | NP_000517.2:n.766-70del | |
| NM_000526.5:c.766-70del MANE Select | NP_000517.3:n.766-70del |