Linked Data
gnomAD v4:
4-67740167-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740171del , CM000666.2:g.67740171del | GRCh38 |
| NC_000004.11:g.68605889del , CM000666.1:g.68605889del | GRCh37 |
| NC_000004.10:g.68288484del | NCBI36 |
| NG_009293.1:g.20919del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.*312del MANE Select | ENSP00000226413.5:n.*312del | |
| ENST00000226413.4:c.*312del | ENSP00000226413.4:n.*312del | |
| NM_000406.2:c.*312del | NP_000397.1:n.*312del | |
| NM_001012763.1:c.*421del | NP_001012781.1:n.*421del | |
| NM_000406.3:c.*312del MANE Select | NP_000397.1:n.*312del | |
| NM_001012763.2:c.*421del | NP_001012781.1:n.*421del |