HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273472G>C , CM000674.2:g.4273472G>C | GRCh38 |
NC_000012.11:g.4382638G>C , CM000674.1:g.4382638G>C | GRCh37 |
NC_000012.10:g.4252899G>C | NCBI36 |
NG_034254.1:g.4737G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-41+219G>C (CCND2) | ENSP00000502597.1:n.-41+219G>C | |
ENST00000676411.1:c.-40-529G>C (CCND2) | ENSP00000502654.1:n.-40-529G>C | |
NR_125790.1:n.126+2587C>G (CCND2-AS1) | ||
NR_149145.1:n.182+1824C>G (CCND2-AS1) | ||
NR_149146.1:n.182+1824C>G (CCND2-AS1) |