Canonical Allele Identifier: CA2013084101
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273524T= , CM000674.2:g.4273524T= GRCh38
NC_000012.11:g.4382690T= , CM000674.1:g.4382690T= GRCh37
NC_000012.10:g.4252951T= NCBI36
NG_034254.1:g.4789T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+271T= (CCND2) ENSP00000502597.1:n.-41+271T=
ENST00000676411.1:c.-40-477T= (CCND2) ENSP00000502654.1:n.-40-477T=
NR_125790.1:n.126+2535A= (CCND2-AS1)
NR_149145.1:n.182+1772A= (CCND2-AS1)
NR_149146.1:n.182+1772A= (CCND2-AS1)