HGVS | Genome Assembly |
---|---|
NC_000005.10:g.23508989T= , CM000667.2:g.23508989T= | GRCh38 |
NC_000005.9:g.23509098T= , CM000667.1:g.23509098T= | GRCh37 |
NC_000005.8:g.23544855T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000502755.6:c.-45T= | ENSP00000425471.2:n.-45T= | |
ENST00000296682.4:c.-45T= MANE Select | ENSP00000296682.4:n.-45T= | |
ENST00000296682.3:c.-45T= | ENSP00000296682.3:n.-45T= | |
ENST00000502755.5:c.-45T= | ENSP00000425471.1:n.-45T= | |
ENST00000635252.1:c.17-931T= | ENSP00000489227.1:n.17-931T= | |
NM_020227.2:c.-45T= | NP_064612.2:n.-45T= | |
NM_020227.3:c.-45T= | NP_064612.2:n.-45T= | |
NM_001376900.1:c.-45T= | NP_001363829.1:n.-45T= | |
NM_020227.4:c.-45T= MANE Select | NP_064612.2:n.-45T= |