Canonical Allele Identifier: CA2013084065
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863810872
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273442T>G , CM000674.2:g.4273442T>G GRCh38
NC_000012.11:g.4382608T>G , CM000674.1:g.4382608T>G GRCh37
NC_000012.10:g.4252869T>G NCBI36
NG_034254.1:g.4707T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+189T>G (CCND2) ENSP00000502597.1:n.-41+189T>G
ENST00000676411.1:c.-40-559T>G (CCND2) ENSP00000502654.1:n.-40-559T>G
NR_125790.1:n.126+2617A>C (CCND2-AS1)
NR_149145.1:n.182+1854A>C (CCND2-AS1)
NR_149146.1:n.182+1854A>C (CCND2-AS1)
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