Linked Data
gnomAD v4:
15-74751881-CCAG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74751882_74751884del , CM000677.2:g.74751882_74751884del | GRCh38 |
| NC_000015.9:g.75044223_75044225del , CM000677.1:g.75044223_75044225del | GRCh37 |
| NC_000015.8:g.72831276_72831278del | NCBI36 |
| NG_008431.1:g.34341_34343del | |
| NG_008431.2:g.34341_34343del | |
| NG_061543.1:g.8038_8040del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.1042+28_1042+30del MANE Select | ENSP00000342007.4:n.1042+28_1042+30del | |
| ENST00000343932.4:c.1042+28_1042+30del | ENSP00000342007.4:n.1042+28_1042+30del | |
| NM_000761.4:c.1042+28_1042+30del | NP_000752.2:n.1042+28_1042+30del | |
| NM_000761.5:c.1042+28_1042+30del MANE Select | NP_000752.2:n.1042+28_1042+30del |