Linked Data
dbSNP Id:
rs1841382295
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62492137del , CM000672.2:g.62492137del | GRCh38 |
| NC_000010.10:g.64251896del , CM000672.1:g.64251896del | GRCh37 |
| NC_000010.9:g.63921902del | NCBI36 |
| NG_021209.1:g.122981del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647733.1:c.981+32340del | ENSP00000502188.1:n.981+32340del | |
| ENST00000410046.7:c.981+32340del | ENSP00000387091.3:n.981+32340del | |
| NM_199451.2:c.981+32340del | NP_955523.1:n.981+32340del | |
| XM_017015937.2:c.981+32340del | XP_016871426.1:n.981+32340del | |
| NM_199451.3:c.981+32340del | NP_955523.1:n.981+32340del |