Linked Data
gnomAD v4:
7-155812311-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155812316del , CM000669.2:g.155812316del | GRCh38 |
| NC_000007.13:g.155605010del , CM000669.1:g.155605010del | GRCh37 |
| NC_000007.12:g.155297771del | NCBI36 |
| NG_007504.2:g.4962del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297261.7:c.-190del MANE Select | ENSP00000297261.2:n.-190del | |
| NM_000193.4:c.-190del MANE Select | NP_000184.1:n.-190del |