Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273747T= , CM000674.2:g.4273747T= | GRCh38 |
| NC_000012.11:g.4382913T= , CM000674.1:g.4382913T= | GRCh37 |
| NC_000012.10:g.4253174T= | NCBI36 |
| NG_034254.1:g.5012T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-40-254T= (CCND2) | ENSP00000502597.1:n.-40-254T= | |
| ENST00000676411.1:c.-40-254T= (CCND2) | ENSP00000502654.1:n.-40-254T= | |
| NM_001759.3:c.-294T= (CCND2) | NP_001750.1:n.-294T= | |
| NR_125790.1:n.126+2312A= (CCND2-AS1) | ||
| XM_005253813.3:c.-294T= (CCND2) | XP_005253870.1:n.-294T= | |
| NR_149145.1:n.182+1549A= (CCND2-AS1) | ||
| NR_149146.1:n.182+1549A= (CCND2-AS1) |