Linked Data
dbSNP Id:
rs1441341915
gnomAD v4:
12-4273738-C-G
MyVariant Identifiers:
chr12:g.4273738C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273738C>G , CM000674.2:g.4273738C>G | GRCh38 |
| NC_000012.11:g.4382904C>G , CM000674.1:g.4382904C>G | GRCh37 |
| NC_000012.10:g.4253165C>G | NCBI36 |
| NG_034254.1:g.5003C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000676279.1:c.-40-263C>G (CCND2) | ENSP00000502597.1:n.-40-263C>G | |
| ENST00000676411.1:c.-40-263C>G (CCND2) | ENSP00000502654.1:n.-40-263C>G | |
| NM_001759.3:c.-303C>G (CCND2) | NP_001750.1:n.-303C>G | |
| NR_125790.1:n.126+2321G>C (CCND2-AS1) | ||
| XM_005253813.3:c.-303C>G (CCND2) | XP_005253870.1:n.-303C>G | |
| NR_149145.1:n.182+1558G>C (CCND2-AS1) | ||
| NR_149146.1:n.182+1558G>C (CCND2-AS1) |