Canonical Allele Identifier: CA944199132
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

gnomAD v3: 12-4273548-A-C
gnomAD v4: 12-4273548-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273548A>C , CM000674.2:g.4273548A>C GRCh38
NC_000012.11:g.4382714A>C , CM000674.1:g.4382714A>C GRCh37
NC_000012.10:g.4252975A>C NCBI36
NG_034254.1:g.4813A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+295A>C (CCND2) ENSP00000502597.1:n.-41+295A>C
ENST00000676411.1:c.-40-453A>C (CCND2) ENSP00000502654.1:n.-40-453A>C
NR_125790.1:n.126+2511T>G (CCND2-AS1)
NR_149145.1:n.182+1748T>G (CCND2-AS1)
NR_149146.1:n.182+1748T>G (CCND2-AS1)