HGVS | Genome Assembly |
---|---|
NC_000012.12:g.9116314A>G , CM000674.2:g.9116314A>G | GRCh38 |
NC_000012.11:g.9268910A>G , CM000674.1:g.9268910A>G | GRCh37 |
NC_000012.10:g.9160177A>G | NCBI36 |
NG_011717.1:g.4649T>C | |
NG_011717.2:g.4649T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_017018683.1:c.*34-9060A>G | XP_016874172.1:n.*34-9060A>G | |
XM_017018684.1:c.*34-18772A>G | XP_016874173.1:n.*34-18772A>G | |
XM_017018685.1:c.*33+58148A>G | XP_016874174.1:n.*33+58148A>G |