Linked Data
gnomAD v4:
8-118111536-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111539del , CM000670.2:g.118111539del | GRCh38 |
| NC_000008.10:g.119123778del , CM000670.1:g.119123778del | GRCh37 |
| NC_000008.9:g.119192959del | NCBI36 |
| NG_007455.2:g.5283del , LRG_493:g.5283del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-491del MANE Select | ENSP00000367446.3:n.-491del | |
| ENST00000378204.6:c.-491del | ENSP00000367446.2:n.-491del | |
| NM_000127.2:c.-491del , LRG_493t1:c.-491del | NP_000118.2:n.-491del | |
| NM_000127.3:c.-491del MANE Select | NP_000118.2:n.-491del |