Canonical Allele Identifier: CA2013084069
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863810985

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273452del , CM000674.2:g.4273452del GRCh38
NC_000012.11:g.4382618del , CM000674.1:g.4382618del GRCh37
NC_000012.10:g.4252879del NCBI36
NG_034254.1:g.4717del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+199del (CCND2) ENSP00000502597.1:n.-41+199del
ENST00000676411.1:c.-40-549del (CCND2) ENSP00000502654.1:n.-40-549del
NR_125790.1:n.126+2607del (CCND2-AS1)
NR_149145.1:n.182+1844del (CCND2-AS1)
NR_149146.1:n.182+1844del (CCND2-AS1)