Canonical Allele Identifier: CA232171373
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs949644563
gnomAD v3: 12-4273375-A-C
gnomAD v4: 12-4273375-A-C
MyVariant Identifiers: chr12:g.4382541A>C (hg19) chr12:g.4273375A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273375A>C , CM000674.2:g.4273375A>C GRCh38
NC_000012.11:g.4382541A>C , CM000674.1:g.4382541A>C GRCh37
NC_000012.10:g.4252802A>C NCBI36
NG_034254.1:g.4640A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+122A>C (CCND2) ENSP00000502597.1:n.-41+122A>C
ENST00000676411.1:c.-40-626A>C (CCND2) ENSP00000502654.1:n.-40-626A>C
NR_125790.1:n.126+2684T>G (CCND2-AS1)
NR_149145.1:n.182+1921T>G (CCND2-AS1)
NR_149146.1:n.182+1921T>G (CCND2-AS1)
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