HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67482969A>C , CM000673.2:g.67482969A>C | GRCh38 |
NC_000011.9:g.67250440A>C , CM000673.1:g.67250440A>C | GRCh37 |
NC_000011.8:g.67007016A>C | NCBI36 |
NG_008969.1:g.4936A>C , LRG_460:g.4936A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682699.1:c.-190A>C | ENSP00000507935.1:n.-190A>C | |
XM_024448761.1:c.-190A>C | XP_024304529.1:n.-190A>C |