Linked Data
dbSNP Id:
rs1180064994
gnomAD v2:
7-41811799-T-G
gnomAD v3:
7-41772201-T-G
gnomAD v4:
7-41772201-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41772201T>G , CM000669.2:g.41772201T>G | GRCh38 |
| NC_000007.13:g.41811799T>G , CM000669.1:g.41811799T>G | GRCh37 |
| NC_000007.12:g.41778324T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027118.1:n.359-695T>G | ||
| NR_027118.2:n.356-695T>G | ||
| XR_001745185.1:n.964+36487T>G | ||
| XR_001745186.1:n.954+36497T>G |