Linked Data
ClinVar Variation Id:
843795
ClinVar RCV Id:
RCV001046492
dbSNP Id:
rs199422261
gnomAD v4:
3-169765024-T-G
MyVariant Identifiers:
chr3:g.169482812T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169765024T>G , CM000665.2:g.169765024T>G | GRCh38 |
| NC_000003.11:g.169482812T>G , CM000665.1:g.169482812T>G | GRCh37 |
| NC_000003.10:g.170965506T>G | NCBI36 |
| NG_016363.1:g.5037A>C , LRG_347:g.5037A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.37A>C , LRG_347t1:n.37A>C |