HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4273725G>T , CM000674.2:g.4273725G>T | GRCh38 |
NC_000012.11:g.4382891G>T , CM000674.1:g.4382891G>T | GRCh37 |
NC_000012.10:g.4253152G>T | NCBI36 |
NG_034254.1:g.4990G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000676279.1:c.-40-276G>T (CCND2) | ENSP00000502597.1:n.-40-276G>T | |
ENST00000676411.1:c.-40-276G>T (CCND2) | ENSP00000502654.1:n.-40-276G>T | |
NR_125790.1:n.126+2334C>A (CCND2-AS1) | ||
NR_149145.1:n.182+1571C>A (CCND2-AS1) | ||
NR_149146.1:n.182+1571C>A (CCND2-AS1) |