HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273513T= , CM000674.2:g.4273513T= | GRCh38 |
NC_000012.11:g.4382679T= , CM000674.1:g.4382679T= | GRCh37 |
NC_000012.10:g.4252940T= | NCBI36 |
NG_034254.1:g.4778T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-41+260T= (CCND2) | ENSP00000502597.1:n.-41+260T= | |
ENST00000676411.1:c.-40-488T= (CCND2) | ENSP00000502654.1:n.-40-488T= | |
NR_125790.1:n.126+2546A= (CCND2-AS1) | ||
NR_149145.1:n.182+1783A= (CCND2-AS1) | ||
NR_149146.1:n.182+1783A= (CCND2-AS1) |