Linked Data
gnomAD v4:
4-55125488-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125490del , CM000666.2:g.55125490del | GRCh38 |
| NC_000004.11:g.55991657del , CM000666.1:g.55991657del | GRCh37 |
| NC_000004.10:g.55686414del | NCBI36 |
| NG_012004.1:g.5107del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-196del MANE Select | ENSP00000263923.4:n.-196del | |
| ENST00000263923.4:c.-196del | ENSP00000263923.4:n.-196del | |
| NM_002253.2:c.-196del | NP_002244.1:n.-196del | |
| NM_002253.3:c.-196del | NP_002244.1:n.-196del | |
| NM_002253.4:c.-196del MANE Select | NP_002244.1:n.-196del |