Linked Data
dbSNP Id:
rs1863815901
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273691G>C , CM000674.2:g.4273691G>C | GRCh38 |
| NC_000012.11:g.4382857G>C , CM000674.1:g.4382857G>C | GRCh37 |
| NC_000012.10:g.4253118G>C | NCBI36 |
| NG_034254.1:g.4956G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-40-310G>C (CCND2) | ENSP00000502597.1:n.-40-310G>C | |
| ENST00000676411.1:c.-40-310G>C (CCND2) | ENSP00000502654.1:n.-40-310G>C | |
| NR_125790.1:n.126+2368C>G (CCND2-AS1) | ||
| NR_149145.1:n.182+1605C>G (CCND2-AS1) | ||
| NR_149146.1:n.182+1605C>G (CCND2-AS1) |