HGVS | Genome Assembly |
---|---|
NC_000007.14:g.130910288A>G , CM000669.2:g.130910288A>G | GRCh38 |
NC_000007.13:g.130595047A>G , CM000669.1:g.130595047A>G | GRCh37 |
NC_000007.12:g.130245587A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_034120.1:n.403+1822T>C | ||
NR_110472.1:n.403+1822T>C | ||
NR_110473.1:n.403+1822T>C | ||
NR_170175.1:n.1765+1822T>C | ||
NR_170176.1:n.1599-25892T>C |