Linked Data
gnomAD v4:
12-4273677-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273677G>T , CM000674.2:g.4273677G>T | GRCh38 |
| NC_000012.11:g.4382843G>T , CM000674.1:g.4382843G>T | GRCh37 |
| NC_000012.10:g.4253104G>T | NCBI36 |
| NG_034254.1:g.4942G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-40-324G>T (CCND2) | ENSP00000502597.1:n.-40-324G>T | |
| ENST00000676411.1:c.-40-324G>T (CCND2) | ENSP00000502654.1:n.-40-324G>T | |
| NR_125790.1:n.126+2382C>A (CCND2-AS1) | ||
| NR_149145.1:n.182+1619C>A (CCND2-AS1) | ||
| NR_149146.1:n.182+1619C>A (CCND2-AS1) |