Canonical Allele Identifier: CA2013084009
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863809287
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273328T>C , CM000674.2:g.4273328T>C GRCh38
NC_000012.11:g.4382494T>C , CM000674.1:g.4382494T>C GRCh37
NC_000012.10:g.4252755T>C NCBI36
NG_034254.1:g.4593T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+75T>C (CCND2) ENSP00000502597.1:n.-41+75T>C
ENST00000676411.1:c.-40-673T>C (CCND2) ENSP00000502654.1:n.-40-673T>C
NR_125790.1:n.126+2731A>G (CCND2-AS1)
NR_149145.1:n.182+1968A>G (CCND2-AS1)
NR_149146.1:n.182+1968A>G (CCND2-AS1)
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