HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106940310A= , CM000685.2:g.106940310A= | GRCh38 |
NC_000023.10:g.106183540A= , CM000685.1:g.106183540A= | GRCh37 |
NC_000023.9:g.106070196A= | NCBI36 |
NG_016392.1:g.64935T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000604604.1:c.111+52920T= | ||
XM_005262190.3:c.*1169T= | XP_005262247.1:n.*1169T= | |
XM_006724691.2:c.*1169T= | XP_006724754.1:n.*1169T= | |
XM_011531027.2:c.*1169T= | XP_011529329.1:n.*1169T= | |
XM_017029844.1:c.*1242T= | XP_016885333.1:n.*1242T= |