Linked Data
gnomAD v4:
X-68829649-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68829651del , CM000685.2:g.68829651del | GRCh38 |
| NC_000023.10:g.68049494del , CM000685.1:g.68049494del | GRCh37 |
| NC_000023.9:g.67966219del | NCBI36 |
| NG_008887.1:g.5655del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.-126del MANE Select | ENSP00000204961.4:n.-126del | |
| ENST00000204961.4:c.-126del | ENSP00000204961.4:n.-126del | |
| NM_004429.4:c.-126del | NP_004420.1:n.-126del | |
| NM_004429.5:c.-126del MANE Select | NP_004420.1:n.-126del |