Linked Data
gnomAD v4:
22-27750386-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750388del , CM000684.2:g.27750388del | GRCh38 |
| NC_000022.10:g.28146376del , CM000684.1:g.28146376del | GRCh37 |
| NC_000022.9:g.26476376del | NCBI36 |
| NG_023258.1:g.56112del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.1016del | ||
| ENST00000302326.5:c.*528del MANE Select | ENSP00000304956.4:n.*528del | |
| ENST00000302326.4:c.*528del | ENSP00000304956.4:n.*528del | |
| ENST00000424656.1:c.456-159del | ||
| NM_002430.2:c.*528del | NP_002421.3:n.*528del | |
| NM_002430.3:c.*528del MANE Select | NP_002421.3:n.*528del |