HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58692453T>C , CM000679.2:g.58692453T>C | GRCh38 |
NC_000017.10:g.56769814T>C , CM000679.1:g.56769814T>C | GRCh37 |
NC_000017.9:g.54124813T>C | NCBI36 |
NG_023199.1:g.4852T>C , LRG_314:g.4852T>C | |
NG_047169.1:g.4627A>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_006722001.4:c.-191T>C | XP_006722064.1:n.-191T>C | |
XM_006722002.4:c.-191T>C | XP_006722065.1:n.-191T>C | |
XR_934513.3:n.314T>C | ||
XR_934514.3:n.314T>C |