Linked Data
gnomAD v4:
7-155463209-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155463213del , CM000669.2:g.155463213del | GRCh38 |
| NC_000007.13:g.155255908del , CM000669.1:g.155255908del | GRCh37 |
| NC_000007.12:g.154948669del | NCBI36 |
| NG_007124.1:g.11494del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297375.4:c.*526del MANE Select | ENSP00000297375.4:n.*526del | |
| NM_001427.3:c.*526del | NP_001418.2:n.*526del | |
| NM_001427.4:c.*526del MANE Select | NP_001418.2:n.*526del |