Canonical Allele Identifier: CA2794362663
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273517G>T , CM000674.2:g.4273517G>T GRCh38
NC_000012.11:g.4382683G>T , CM000674.1:g.4382683G>T GRCh37
NC_000012.10:g.4252944G>T NCBI36
NG_034254.1:g.4782G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+264G>T (CCND2) ENSP00000502597.1:n.-41+264G>T
ENST00000676411.1:c.-40-484G>T (CCND2) ENSP00000502654.1:n.-40-484G>T
NR_125790.1:n.126+2542C>A (CCND2-AS1)
NR_149145.1:n.182+1779C>A (CCND2-AS1)
NR_149146.1:n.182+1779C>A (CCND2-AS1)