Canonical Allele Identifier: CA2013084257
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863816789

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273729dup , CM000674.2:g.4273729dup GRCh38
NC_000012.11:g.4382895dup , CM000674.1:g.4382895dup GRCh37
NC_000012.10:g.4253156dup NCBI36
NG_034254.1:g.4994dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-272dup (CCND2) ENSP00000502597.1:n.-40-272dup
ENST00000676411.1:c.-40-272dup (CCND2) ENSP00000502654.1:n.-40-272dup
NR_125790.1:n.126+2330dup (CCND2-AS1)
NR_149145.1:n.182+1567dup (CCND2-AS1)
NR_149146.1:n.182+1567dup (CCND2-AS1)