Linked Data
gnomAD v4:
5-71719596-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719598del , CM000667.2:g.71719598del | GRCh38 |
| NC_000005.9:g.71015425del , CM000667.1:g.71015425del | GRCh37 |
| NC_000005.8:g.71051181del | NCBI36 |
| NG_015988.1:g.5436del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.159+146del MANE Select | ENSP00000296777.4:n.159+146del | |
| ENST00000296777.4:c.159+146del | ENSP00000296777.4:n.159+146del | |
| ENST00000513096.1:n.20del | ||
| NM_004291.3:c.159+146del | NP_004282.1:n.159+146del | |
| NM_004291.4:c.159+146del MANE Select | NP_004282.1:n.159+146del |