HGVS | Genome Assembly |
---|---|
NC_000014.9:g.64338283A= , CM000676.2:g.64338283A= | GRCh38 |
NC_000014.8:g.64805001A= , CM000676.1:g.64805001A= | GRCh37 |
NC_000014.7:g.63874754A= | NCBI36 |
NG_011535.1:g.5268T= |
HGVS | Amino-acid Change |
---|---|
NM_001291712.1:c.-1461T= | NP_001278641.1:n.-1461T= |
NM_001291712.2:c.-1461T= | NP_001278641.1:n.-1461T= |
NM_001291723.1:c.-476T= | NP_001278652.1:n.-476T= |
NR_073496.1:n.268T= | |
NR_073496.2:n.331T= | |
XM_017021079.1:c.-784T= | XP_016876568.1:n.-784T= |
XM_017021080.1:c.-1593T= | XP_016876569.1:n.-1593T= |
XM_017021081.1:c.-689T= | XP_016876570.1:n.-689T= |
XM_017021084.1:c.-784T= | XP_016876573.1:n.-784T= |