HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273398G= , CM000674.2:g.4273398G= | GRCh38 |
NC_000012.11:g.4382564G= , CM000674.1:g.4382564G= | GRCh37 |
NC_000012.10:g.4252825G= | NCBI36 |
NG_034254.1:g.4663G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-41+145G= (CCND2) | ENSP00000502597.1:n.-41+145G= | |
ENST00000676411.1:c.-40-603G= (CCND2) | ENSP00000502654.1:n.-40-603G= | |
NR_125790.1:n.126+2661C= (CCND2-AS1) | ||
NR_149145.1:n.182+1898C= (CCND2-AS1) | ||
NR_149146.1:n.182+1898C= (CCND2-AS1) |