HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273469A>G , CM000674.2:g.4273469A>G | GRCh38 |
NC_000012.11:g.4382635A>G , CM000674.1:g.4382635A>G | GRCh37 |
NC_000012.10:g.4252896A>G | NCBI36 |
NG_034254.1:g.4734A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-41+216A>G (CCND2) | ENSP00000502597.1:n.-41+216A>G | |
ENST00000676411.1:c.-40-532A>G (CCND2) | ENSP00000502654.1:n.-40-532A>G | |
NR_125790.1:n.126+2590T>C (CCND2-AS1) | ||
NR_149145.1:n.182+1827T>C (CCND2-AS1) | ||
NR_149146.1:n.182+1827T>C (CCND2-AS1) |