Linked Data
dbSNP Id:
rs1777957722
gnomAD v3:
3-169764663-G-C
gnomAD v4:
3-169764663-G-C
MyVariant Identifiers:
chr3:g.169482451G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764663G>C , CM000665.2:g.169764663G>C | GRCh38 |
| NC_000003.11:g.169482451G>C , CM000665.1:g.169482451G>C | GRCh37 |
| NC_000003.10:g.170965145G>C | NCBI36 |
| NG_016363.1:g.5398C>G , LRG_347:g.5398C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.398C>G , LRG_347t1:n.398C>G |