Canonical Allele Identifier: CA2013084032
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273375A= , CM000674.2:g.4273375A= GRCh38
NC_000012.11:g.4382541A= , CM000674.1:g.4382541A= GRCh37
NC_000012.10:g.4252802A= NCBI36
NG_034254.1:g.4640A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+122A= (CCND2) ENSP00000502597.1:n.-41+122A=
ENST00000676411.1:c.-40-626A= (CCND2) ENSP00000502654.1:n.-40-626A=
NR_125790.1:n.126+2684T= (CCND2-AS1)
NR_149145.1:n.182+1921T= (CCND2-AS1)
NR_149146.1:n.182+1921T= (CCND2-AS1)
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