HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273684A>C , CM000674.2:g.4273684A>C | GRCh38 |
NC_000012.11:g.4382850A>C , CM000674.1:g.4382850A>C | GRCh37 |
NC_000012.10:g.4253111A>C | NCBI36 |
NG_034254.1:g.4949A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-40-317A>C (CCND2) | ENSP00000502597.1:n.-40-317A>C | |
ENST00000676411.1:c.-40-317A>C (CCND2) | ENSP00000502654.1:n.-40-317A>C | |
NR_125790.1:n.126+2375T>G (CCND2-AS1) | ||
NR_149145.1:n.182+1612T>G (CCND2-AS1) | ||
NR_149146.1:n.182+1612T>G (CCND2-AS1) |