HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2001815G>A , CM000673.2:g.2001815G>A | GRCh38 |
NC_000011.9:g.2023045G>A , CM000673.1:g.2023045G>A | GRCh37 |
NC_000011.8:g.1979621G>A | NCBI36 |
NG_016165.1:g.1021C>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_011520273.1:c.498-9726G>A | XP_011518575.1:n.498-9726G>A | |
XM_011520274.1:c.492-9726G>A | XP_011518576.1:n.492-9726G>A | |
XM_011520275.1:c.498-9726G>A | XP_011518577.1:n.498-9726G>A | |
XM_011520275.2:c.498-9726G>A | XP_011518577.1:n.498-9726G>A | |
NM_001400176.1:c.498-9726G>A | NP_001387105.1:n.498-9726G>A |