HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764934T>G , CM000665.2:g.169764934T>G | GRCh38 |
NC_000003.11:g.169482722T>G , CM000665.1:g.169482722T>G | GRCh37 |
NC_000003.10:g.170965416T>G | NCBI36 |
NG_016363.1:g.5127A>C , LRG_347:g.5127A>C |
HGVS | Amino-acid change | |
---|---|---|
NR_001566.1:n.127A>C , LRG_347t1:n.127A>C |