Linked Data
gnomAD v4:
7-152675961-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152675966del , CM000669.2:g.152675966del | GRCh38 |
| NC_000007.13:g.152373051del , CM000669.1:g.152373051del | GRCh37 |
| NC_000007.12:g.152003984del | NCBI36 |
| NG_027988.1:g.5204del | |
| NG_027988.2:g.5204del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.-48+79del | ENSP00000513758.1:n.-48+79del | |
| ENST00000698507.1:n.107+79del | ||
| ENST00000359321.2:c.39+79del MANE Select | ENSP00000352271.1:n.39+79del | |
| ENST00000359321.1:c.39+79del | ENSP00000352271.1:n.39+79del | |
| NM_005431.1:c.39+79del | NP_005422.1:n.39+79del | |
| NM_005431.2:c.39+79del MANE Select | NP_005422.1:n.39+79del |