HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764872C>G , CM000665.2:g.169764872C>G | GRCh38 |
NC_000003.11:g.169482660C>G , CM000665.1:g.169482660C>G | GRCh37 |
NC_000003.10:g.170965354C>G | NCBI36 |
NG_016363.1:g.5189G>C , LRG_347:g.5189G>C |
HGVS | Amino-acid change | |
---|---|---|
NR_001566.1:n.189G>C , LRG_347t1:n.189G>C |