Linked Data
gnomAD v4:
6-1610020-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610020_1610021insT , CM000668.2:g.1610020_1610021insT | GRCh38 |
| NC_000006.11:g.1610255_1610256insT , CM000668.1:g.1610255_1610256insT | GRCh37 |
| NC_000006.10:g.1555254_1555255insT | NCBI36 |
| NG_009368.1:g.4575_4576insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.-426_-425insT MANE Select | ENSP00000493906.1:n.-426_-425insT | |
| ENST00000380874.3:c.-426_-425insT | ENSP00000370256.2:n.-426_-425insT | |
| NM_001453.3:c.-426_-425insT MANE Select | NP_001444.2:n.-426_-425insT |