HGVS | Genome Assembly |
---|---|
NC_000012.12:g.77781581C>G , CM000674.2:g.77781581C>G | GRCh38 |
NC_000012.11:g.78175361C>G , CM000674.1:g.78175361C>G | GRCh37 |
NC_000012.10:g.76699492C>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000550042.2:c.73-158738C>G | ENSP00000489639.1:n.73-158738C>G | |
XM_011538942.1:c.73-158738C>G | XP_011537244.1:n.73-158738C>G | |
XR_945128.1:n.433-1682C>G | ||
XR_945129.1:n.417-1682C>G | ||
XM_017020166.2:c.73-158738C>G | XP_016875655.1:n.73-158738C>G | |
XM_017020167.1:c.73-158738C>G | XP_016875656.1:n.73-158738C>G |