Linked Data
dbSNP Id:
rs1170392745
gnomAD v2:
12-4383050-T-G
gnomAD v3:
12-4273884-T-G
gnomAD v4:
12-4273884-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273884T>G , CM000674.2:g.4273884T>G | GRCh38 |
| NC_000012.11:g.4383050T>G , CM000674.1:g.4383050T>G | GRCh37 |
| NC_000012.10:g.4253311T>G | NCBI36 |
| NG_034254.1:g.5149T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261254.8:c.-157T>G (CCND2) MANE Select | ENSP00000261254.3:n.-157T>G | |
| ENST00000536537.2:n.123T>G (CCND2) | ||
| ENST00000648100.1:c.-157T>G | ENSP00000497536.1:n.-157T>G | |
| ENST00000674624.1:c.-157T>G | ENSP00000501898.1:n.-157T>G | |
| ENST00000675880.1:c.-157T>G (CCND2) | ENSP00000502508.1:n.-157T>G | |
| ENST00000676279.1:c.-40-117T>G (CCND2) | ENSP00000502597.1:n.-40-117T>G | |
| ENST00000676411.1:c.-40-117T>G (CCND2) | ENSP00000502654.1:n.-40-117T>G | |
| ENST00000261254.7:c.-157T>G (CCND2) | ENSP00000261254.3:n.-157T>G | |
| NM_001759.3:c.-157T>G (CCND2) | NP_001750.1:n.-157T>G | |
| NR_125790.1:n.126+2175A>C (CCND2-AS1) | ||
| XM_005253813.3:c.-157T>G (CCND2) | XP_005253870.1:n.-157T>G | |
| NR_149145.1:n.182+1412A>C (CCND2-AS1) | ||
| NR_149146.1:n.182+1412A>C (CCND2-AS1) | ||
| NM_001759.4:c.-157T>G (CCND2) MANE Select | NP_001750.1:n.-157T>G |