HGVS | Genome Assembly |
---|---|
NC_000015.10:g.55498394A= , CM000677.2:g.55498394A= | GRCh38 |
NC_000015.9:g.55790592A= , CM000677.1:g.55790592A= | GRCh37 |
NC_000015.8:g.53577884A= | NCBI36 |
NG_021213.1:g.14841T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000321149.7:c.-65T= (DNAAF4) MANE Select | ENSP00000323275.3:n.-65T= | |
ENST00000348518.4:c.-65T= (DNAAF4) | ENSP00000299561.5:n.-65T= | |
NM_001033559.2:c.-65T= (DNAAF4) | NP_001028731.1:n.-65T= | |
NM_001033560.1:c.-65T= (DNAAF4) | NP_001028732.1:n.-65T= | |
NM_130810.3:c.-65T= (DNAAF4) | NP_570722.2:n.-65T= | |
NR_037923.1:n.191T= (DNAAF4-CCPG1) | ||
NM_130810.4:c.-65T= (DNAAF4) MANE Select | NP_570722.2:n.-65T= | |
NM_001033559.3:c.-65T= (DNAAF4) | NP_001028731.1:n.-65T= | |
NM_001033560.2:c.-65T= (DNAAF4) | NP_001028732.1:n.-65T= |