Linked Data
gnomAD v4:
2-27323096-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27323098del , CM000664.2:g.27323098del | GRCh38 |
| NC_000002.11:g.27545965del , CM000664.1:g.27545965del | GRCh37 |
| NC_000002.10:g.27399469del | NCBI36 |
| NG_008075.1:g.4468del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357186.10:c.18+1336del | ENSP00000349713.6:n.18+1336del | |
| ENST00000380044.5:c.-51del | ENSP00000369383.1:n.-51del | |
| ENST00000405076.5:c.-51del | ENSP00000385175.1:n.-51del | |
| ENST00000621183.4:n.6del | ||
| NM_002437.4:c.-51del | NP_002428.1:n.-51del | |
| XM_005264327.2:c.-175del | XP_005264384.1:n.-175del |