Linked Data
dbSNP Id:
rs2073451877
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228262del , CM000679.2:g.66228262del | GRCh38 |
| NC_000017.10:g.64224380del , CM000679.1:g.64224380del | GRCh37 |
| NC_000017.9:g.61654842del | NCBI36 |
| NG_012045.1:g.6179del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205948.11:c.65-64del MANE Select | ENSP00000205948.6:n.65-64del | |
| ENST00000205948.10:c.65-64del | ENSP00000205948.6:n.65-64del | |
| ENST00000577982.1:c.65-64del | ENSP00000464301.1:n.65-64del | |
| ENST00000581797.5:c.-116-64del | ENSP00000463553.1:n.-116-64del | |
| NM_000042.2:c.65-64del | NP_000033.2:n.65-64del | |
| NM_000042.3:c.65-64del MANE Select | NP_000033.2:n.65-64del |