Linked Data
dbSNP Id:
rs1340568882
gnomAD v2:
7-41811869-C-A
gnomAD v3:
7-41772271-C-A
gnomAD v4:
7-41772271-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41772271C>A , CM000669.2:g.41772271C>A | GRCh38 |
| NC_000007.13:g.41811869C>A , CM000669.1:g.41811869C>A | GRCh37 |
| NC_000007.12:g.41778394C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027118.1:n.359-625C>A | ||
| NR_027118.2:n.356-625C>A | ||
| XR_001745185.1:n.964+36557C>A | ||
| XR_001745186.1:n.954+36567C>A |