Linked Data
dbSNP Id:
rs1019621688
gnomAD v2:
12-4382901-T-C
gnomAD v3:
12-4273735-T-C
gnomAD v4:
12-4273735-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273735T>C , CM000674.2:g.4273735T>C | GRCh38 |
| NC_000012.11:g.4382901T>C , CM000674.1:g.4382901T>C | GRCh37 |
| NC_000012.10:g.4253162T>C | NCBI36 |
| NG_034254.1:g.5000T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-40-266T>C (CCND2) | ENSP00000502597.1:n.-40-266T>C | |
| ENST00000676411.1:c.-40-266T>C (CCND2) | ENSP00000502654.1:n.-40-266T>C | |
| NR_125790.1:n.126+2324A>G (CCND2-AS1) | ||
| XM_005253813.3:c.-306T>C (CCND2) | XP_005253870.1:n.-306T>C | |
| NR_149145.1:n.182+1561A>G (CCND2-AS1) | ||
| NR_149146.1:n.182+1561A>G (CCND2-AS1) |