Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273529T>C , CM000674.2:g.4273529T>C | GRCh38 |
| NC_000012.11:g.4382695T>C , CM000674.1:g.4382695T>C | GRCh37 |
| NC_000012.10:g.4252956T>C | NCBI36 |
| NG_034254.1:g.4794T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-41+276T>C (CCND2) | ENSP00000502597.1:n.-41+276T>C | |
| ENST00000676411.1:c.-40-472T>C (CCND2) | ENSP00000502654.1:n.-40-472T>C | |
| NR_125790.1:n.126+2530A>G (CCND2-AS1) | ||
| NR_149145.1:n.182+1767A>G (CCND2-AS1) | ||
| NR_149146.1:n.182+1767A>G (CCND2-AS1) |