Linked Data
dbSNP Id:
rs61731957
gnomAD v2:
12-4383375-A-G
gnomAD v3:
12-4274209-A-G
gnomAD v4:
12-4274209-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4274209A>G , CM000674.2:g.4274209A>G | GRCh38 |
| NC_000012.11:g.4383375A>G , CM000674.1:g.4383375A>G | GRCh37 |
| NC_000012.10:g.4253636A>G | NCBI36 |
| NG_034254.1:g.5474A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261254.8:c.169A>G (CCND2) MANE Select | ENSP00000261254.3:p.Arg57Gly | |
| ENST00000536537.2:n.448A>G (CCND2) | ||
| ENST00000648100.1:c.169A>G | ENSP00000497536.1:p.Arg57Gly | |
| ENST00000674624.1:c.169A>G | ENSP00000501898.1:p.Arg57Gly | |
| ENST00000675880.1:c.169A>G (CCND2) | ENSP00000502508.1:p.Arg57Gly | |
| ENST00000676279.1:c.169A>G (CCND2) | ENSP00000502597.1:p.Arg57Gly | |
| ENST00000676411.1:c.169A>G (CCND2) | ENSP00000502654.1:p.Arg57Gly | |
| ENST00000261254.7:c.169A>G (CCND2) | ENSP00000261254.3:p.Arg57Gly | |
| NM_001759.3:c.169A>G (CCND2) | NP_001750.1:p.Arg57Gly | |
| NR_125790.1:n.126+1850T>C (CCND2-AS1) | ||
| XM_005253813.3:c.169A>G (CCND2) | XP_005253870.1:p.Arg57Gly | |
| NR_149145.1:n.182+1087T>C (CCND2-AS1) | ||
| NR_149146.1:n.182+1087T>C (CCND2-AS1) | ||
| NM_001759.4:c.169A>G (CCND2) MANE Select | NP_001750.1:p.Arg57Gly |