Linked Data
gnomAD v4:
X-68829764-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68829765del , CM000685.2:g.68829765del | GRCh38 |
| NC_000023.10:g.68049608del , CM000685.1:g.68049608del | GRCh37 |
| NC_000023.9:g.67966333del | NCBI36 |
| NG_008887.1:g.5769del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.-12del MANE Select | ENSP00000204961.4:n.-12del | |
| ENST00000204961.4:c.-12del | ENSP00000204961.4:n.-12del | |
| NM_004429.4:c.-12del | NP_004420.1:n.-12del | |
| NM_004429.5:c.-12del MANE Select | NP_004420.1:n.-12del |