Linked Data
dbSNP Id:
rs761448528
gnomAD v2:
12-4383048-CCTT-C
gnomAD v3:
12-4273882-CCTT-C
gnomAD v4:
12-4273882-CCTT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4273885_4273887del , CM000674.2:g.4273885_4273887del | GRCh38 |
| NC_000012.11:g.4383051_4383053del , CM000674.1:g.4383051_4383053del | GRCh37 |
| NC_000012.10:g.4253312_4253314del | NCBI36 |
| NG_034254.1:g.5150_5152del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261254.8:c.-156_-154del (CCND2) MANE Select | ENSP00000261254.3:n.-156_-154del | |
| ENST00000536537.2:n.124_126del (CCND2) | ||
| ENST00000648100.1:c.-156_-154del | ENSP00000497536.1:n.-156_-154del | |
| ENST00000674624.1:c.-156_-154del | ENSP00000501898.1:n.-156_-154del | |
| ENST00000675880.1:c.-156_-154del (CCND2) | ENSP00000502508.1:n.-156_-154del | |
| ENST00000676279.1:c.-40-116_-40-114del (CCND2) | ENSP00000502597.1:n.-40-116_-40-114del | |
| ENST00000676411.1:c.-40-116_-40-114del (CCND2) | ENSP00000502654.1:n.-40-116_-40-114del | |
| ENST00000261254.7:c.-156_-154del (CCND2) | ENSP00000261254.3:n.-156_-154del | |
| NM_001759.3:c.-156_-154del (CCND2) | NP_001750.1:n.-156_-154del | |
| NR_125790.1:n.126+2174_126+2176del (CCND2-AS1) | ||
| XM_005253813.3:c.-156_-154del (CCND2) | XP_005253870.1:n.-156_-154del | |
| NR_149145.1:n.182+1411_182+1413del (CCND2-AS1) | ||
| NR_149146.1:n.182+1411_182+1413del (CCND2-AS1) | ||
| NM_001759.4:c.-156_-154del (CCND2) MANE Select | NP_001750.1:n.-156_-154del |