Linked Data
gnomAD v4:
12-4273756-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273756C>T , CM000674.2:g.4273756C>T | GRCh38 |
| NC_000012.11:g.4382922C>T , CM000674.1:g.4382922C>T | GRCh37 |
| NC_000012.10:g.4253183C>T | NCBI36 |
| NG_034254.1:g.5021C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-40-245C>T (CCND2) | ENSP00000502597.1:n.-40-245C>T | |
| ENST00000676411.1:c.-40-245C>T (CCND2) | ENSP00000502654.1:n.-40-245C>T | |
| NM_001759.3:c.-285C>T (CCND2) | NP_001750.1:n.-285C>T | |
| NR_125790.1:n.126+2303G>A (CCND2-AS1) | ||
| XM_005253813.3:c.-285C>T (CCND2) | XP_005253870.1:n.-285C>T | |
| NR_149145.1:n.182+1540G>A (CCND2-AS1) | ||
| NR_149146.1:n.182+1540G>A (CCND2-AS1) |