Linked Data
dbSNP Id:
rs7431368
gnomAD v4:
3-128472098-C-G
MyVariant Identifiers:
chr3:g.128190941C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128472098C>G , CM000665.2:g.128472098C>G | GRCh38 |
| NC_000003.11:g.128190941C>G , CM000665.1:g.128190941C>G | GRCh37 |
| NC_000003.10:g.129673631C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_037890.1:n.1579C>G |