Canonical Allele Identifier: CA2013084121
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273550A= , CM000674.2:g.4273550A= GRCh38
NC_000012.11:g.4382716A= , CM000674.1:g.4382716A= GRCh37
NC_000012.10:g.4252977A= NCBI36
NG_034254.1:g.4815A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+297A= (CCND2) ENSP00000502597.1:n.-41+297A=
ENST00000676411.1:c.-40-451A= (CCND2) ENSP00000502654.1:n.-40-451A=
NR_125790.1:n.126+2509T= (CCND2-AS1)
NR_149145.1:n.182+1746T= (CCND2-AS1)
NR_149146.1:n.182+1746T= (CCND2-AS1)