Canonical Allele Identifier: CA688960665
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1351822828
gnomAD v3: 12-4273714-G-A
gnomAD v4: 12-4273714-G-A
MyVariant Identifiers: chr12:g.4382880G>A (hg19) chr12:g.4273714G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273714G>A , CM000674.2:g.4273714G>A GRCh38
NC_000012.11:g.4382880G>A , CM000674.1:g.4382880G>A GRCh37
NC_000012.10:g.4253141G>A NCBI36
NG_034254.1:g.4979G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-287G>A (CCND2) ENSP00000502597.1:n.-40-287G>A
ENST00000676411.1:c.-40-287G>A (CCND2) ENSP00000502654.1:n.-40-287G>A
NR_125790.1:n.126+2345C>T (CCND2-AS1)
NR_149145.1:n.182+1582C>T (CCND2-AS1)
NR_149146.1:n.182+1582C>T (CCND2-AS1)
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