HGVS | Genome Assembly |
---|---|
NC_000003.12:g.122050448C>T , CM000665.2:g.122050448C>T | GRCh38 |
NC_000003.11:g.121769295C>T , CM000665.1:g.121769295C>T | GRCh37 |
NC_000003.10:g.123251985C>T | NCBI36 |
NG_029928.1:g.87C>T | |
NG_031870.2:g.15107G>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011512739.1:c.-348+9972G>A | XP_011511041.1:n.-348+9972G>A | |
XM_011512739.2:c.-348+9972G>A | XP_011511041.1:n.-348+9972G>A |