HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764950T>C , CM000665.2:g.169764950T>C | GRCh38 |
NC_000003.11:g.169482738T>C , CM000665.1:g.169482738T>C | GRCh37 |
NC_000003.10:g.170965432T>C | NCBI36 |
NG_016363.1:g.5111A>G , LRG_347:g.5111A>G |
HGVS | Amino-acid change | |
---|---|---|
NR_001566.1:n.111A>G , LRG_347t1:n.111A>G |