Linked Data
dbSNP Id:
rs1659111271
gnomAD v2:
1-94884006-CT-C
gnomAD v3:
1-94418450-CT-C
gnomAD v4:
1-94418450-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418451del , CM000663.2:g.94418451del | GRCh38 |
| NC_000001.10:g.94884007del , CM000663.1:g.94884007del | GRCh37 |
| NC_000001.9:g.94656595del | NCBI36 |
| NG_008865.1:g.5075del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.-28del MANE Select | ENSP00000359233.4:n.-28del | |
| NM_001122674.1:c.-28del | NP_001116146.1:n.-28del | |
| NM_002858.3:c.-28del | NP_002849.1:n.-28del | |
| XM_006710802.2:c.-28del | XP_006710865.2:n.-28del | |
| NM_002858.4:c.-28del MANE Select | NP_002849.1:n.-28del | |
| NM_001122674.2:c.-28del | NP_001116146.1:n.-28del |