HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273420G>A , CM000674.2:g.4273420G>A | GRCh38 |
NC_000012.11:g.4382586G>A , CM000674.1:g.4382586G>A | GRCh37 |
NC_000012.10:g.4252847G>A | NCBI36 |
NG_034254.1:g.4685G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-41+167G>A (CCND2) | ENSP00000502597.1:n.-41+167G>A | |
ENST00000676411.1:c.-40-581G>A (CCND2) | ENSP00000502654.1:n.-40-581G>A | |
NR_125790.1:n.126+2639C>T (CCND2-AS1) | ||
NR_149145.1:n.182+1876C>T (CCND2-AS1) | ||
NR_149146.1:n.182+1876C>T (CCND2-AS1) |