Canonical Allele Identifier: CA688960473
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1385317763
gnomAD v3: 12-4273548-A-G
gnomAD v4: 12-4273548-A-G
MyVariant Identifiers: chr12:g.4382714A>G (hg19) chr12:g.4273548A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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