Linked Data
gnomAD v4:
4-67740292-A-AT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740297dup , CM000666.2:g.67740297dup | GRCh38 |
| NC_000004.11:g.68606015dup , CM000666.1:g.68606015dup | GRCh37 |
| NC_000004.10:g.68288610dup | NCBI36 |
| NG_009293.1:g.20794dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.*187dup MANE Select | ENSP00000226413.5:n.*187dup | |
| ENST00000226413.4:c.*187dup | ENSP00000226413.4:n.*187dup | |
| NM_000406.2:c.*187dup | NP_000397.1:n.*187dup | |
| NM_001012763.1:c.*296dup | NP_001012781.1:n.*296dup | |
| NM_000406.3:c.*187dup MANE Select | NP_000397.1:n.*187dup | |
| NM_001012763.2:c.*296dup | NP_001012781.1:n.*296dup |