Linked Data
ClinVar Variation Id:
1331195
ClinVar RCV Id:
RCV001806540
dbSNP Id:
rs3837828
gnomAD v3:
17-35809260-TC-T
gnomAD v4:
17-35809260-TC-T
MyVariant Identifiers:
chr17:g.35809261del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35809264del , CM000679.2:g.35809264del | GRCh38 |
| NC_000017.9:g.31160381del | NCBI36 |
| NG_023279.1:g.4781del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000603067.5:n.7-25001del |