HGVS | Genome Assembly |
---|---|
NC_000020.11:g.54151852T>A , CM000682.2:g.54151852T>A | GRCh38 |
NC_000020.10:g.52768391T>A , CM000682.1:g.52768391T>A | GRCh37 |
NC_000020.9:g.52201798T>A | NCBI36 |
NG_008334.1:g.27126A>T |
HGVS | Amino-acid Change |
---|---|
XM_017027692.2:c.*10+5317A>T | XP_016883181.1:n.*10+5317A>T |