Linked Data
ClinVar Variation Id:
841657
ClinVar RCV Id:
RCV001043924
dbSNP Id:
rs1777963465
MyVariant Identifiers:
chr3:g.169482745G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764957G>A , CM000665.2:g.169764957G>A | GRCh38 |
| NC_000003.11:g.169482745G>A , CM000665.1:g.169482745G>A | GRCh37 |
| NC_000003.10:g.170965439G>A | NCBI36 |
| NG_016363.1:g.5104C>T , LRG_347:g.5104C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.104C>T , LRG_347t1:n.104C>T |