Linked Data
gnomAD v4:
5-140333332-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140333335del , CM000667.2:g.140333335del | GRCh38 |
| NC_000005.9:g.139712920del , CM000667.1:g.139712920del | GRCh37 |
| NC_000005.8:g.139693104del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230990.7:c.*966del MANE Select | ENSP00000230990.6:n.*966del | |
| ENST00000230990.6:c.*966del | ENSP00000230990.6:n.*966del | |
| NM_001945.2:c.*966del | NP_001936.1:n.*966del | |
| NM_001945.3:c.*966del MANE Select | NP_001936.1:n.*966del |