Linked Data
gnomAD v4:
22-27750793-A-AT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750793_27750794insT , CM000684.2:g.27750793_27750794insT | GRCh38 |
| NC_000022.10:g.28146781_28146782insT , CM000684.1:g.28146781_28146782insT | GRCh37 |
| NC_000022.9:g.26476781_26476782insT | NCBI36 |
| NG_023258.1:g.55705_55706insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.609_610insA | ||
| ENST00000302326.5:c.*121_*122insA MANE Select | ENSP00000304956.4:n.*121_*122insA | |
| ENST00000302326.4:c.*121_*122insA | ENSP00000304956.4:n.*121_*122insA | |
| ENST00000424656.1:c.437_438insA | ||
| ENST00000497225.1:n.440_441insA | ||
| NM_002430.2:c.*121_*122insA | NP_002421.3:n.*121_*122insA | |
| NM_002430.3:c.*121_*122insA MANE Select | NP_002421.3:n.*121_*122insA |