Linked Data
gnomAD v4:
16-1986061-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986063del , CM000678.2:g.1986063del | GRCh38 |
| NC_000016.9:g.2036064del , CM000678.1:g.2036064del | GRCh37 |
| NC_000016.8:g.1976065del | NCBI36 |
| NG_016288.1:g.6915del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.*35del | ENSP00000455885.1:n.*35del | |
| ENST00000248114.7:c.*35del MANE Select | ENSP00000248114.6:n.*35del | |
| ENST00000248114.6:c.*35del | ENSP00000248114.6:n.*35del | |
| ENST00000565658.1:n.810del | ||
| ENST00000567719.1:c.*35del | ENSP00000455885.1:n.*35del | |
| ENST00000569451.1:c.*126del | ENSP00000456432.1:n.*126del | |
| NM_005262.2:c.*35del | NP_005253.3:n.*35del | |
| NM_005262.3:c.*35del MANE Select | NP_005253.3:n.*35del |