Linked Data
dbSNP Id:
rs775304836
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21215857_21215860del , CM000674.2:g.21215857_21215860del | GRCh38 |
| NC_000012.11:g.21368791_21368794del , CM000674.1:g.21368791_21368794del | GRCh37 |
| NC_000012.10:g.21260058_21260061del | NCBI36 |
| NG_011745.1:g.89664_89667del , LRG_1022:g.89664_89667del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000256958.3:c.1498-1262_1498-1259del MANE Select | ENSP00000256958.2:n.1498-1262_1498-1259de... | |
| ENST00000256958.2:c.1498-1262_1498-1259del | ENSP00000256958.2:n.1498-1262_1498-1259de... | |
| NM_006446.4:c.1498-1262_1498-1259del , LRG_1022t1:c.1498-1262_1498-1259del | NP_006437.3:n.1498-1262_1498-1259del | |
| NM_006446.5:c.1498-1262_1498-1259del MANE Select | NP_006437.3:n.1498-1262_1498-1259del |