HGVS | Genome Assembly |
---|---|
NC_000011.10:g.117317259T= , CM000673.2:g.117317259T= | GRCh38 |
NC_000011.9:g.117187975T= , CM000673.1:g.117187975T= | GRCh37 |
NC_000011.8:g.116693185T= | NCBI36 |
NG_029372.1:g.3998A= | |
NG_033032.1:g.482T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000525734.5:c.-98+2531T= | ENSP00000436609.1:n.-98+2531T= | |
XM_017017364.1:c.-98+726T= | XP_016872853.1:n.-98+726T= |