Linked Data
dbSNP Id:
rs1408574419
gnomAD v2:
7-41811865-C-G
gnomAD v3:
7-41772267-C-G
gnomAD v4:
7-41772267-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41772267C>G , CM000669.2:g.41772267C>G | GRCh38 |
| NC_000007.13:g.41811865C>G , CM000669.1:g.41811865C>G | GRCh37 |
| NC_000007.12:g.41778390C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027118.1:n.359-629C>G | ||
| NR_027118.2:n.356-629C>G | ||
| XR_001745185.1:n.964+36553C>G | ||
| XR_001745186.1:n.954+36563C>G |