HGVS | Genome Assembly |
---|---|
NC_000006.12:g.12288912G>A , CM000668.2:g.12288912G>A | GRCh38 |
NC_000006.11:g.12289145G>A , CM000668.1:g.12289145G>A | GRCh37 |
NC_000006.10:g.12397131G>A | NCBI36 |
NG_016196.1:g.3617G>A |
HGVS | Amino-acid change | |
---|---|---|
XM_011514330.1:c.-2+417G>A | XP_011512632.1:n.-2+417G>A | |
XM_011514331.1:c.-1-1717G>A | XP_011512633.1:n.-1-1717G>A | |
XM_011514332.1:c.-2+417G>A | XP_011512634.1:n.-2+417G>A | |
XM_011514330.2:c.-2+417G>A | XP_011512632.1:n.-2+417G>A | |
XM_011514331.3:c.-1-1717G>A | XP_011512633.1:n.-1-1717G>A | |
XM_011514332.2:c.-2+417G>A | XP_011512634.1:n.-2+417G>A |