Linked Data
dbSNP Id:
rs1553915617
gnomAD v4:
3-169764954-C-T
MyVariant Identifiers:
chr3:g.169482742C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764954C>T , CM000665.2:g.169764954C>T | GRCh38 |
| NC_000003.11:g.169482742C>T , CM000665.1:g.169482742C>T | GRCh37 |
| NC_000003.10:g.170965436C>T | NCBI36 |
| NG_016363.1:g.5107G>A , LRG_347:g.5107G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.107G>A , LRG_347t1:n.107G>A |