Canonical Allele Identifier: CA2794362659
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273318C>A , CM000674.2:g.4273318C>A GRCh38
NC_000012.11:g.4382484C>A , CM000674.1:g.4382484C>A GRCh37
NC_000012.10:g.4252745C>A NCBI36
NG_034254.1:g.4583C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+65C>A (CCND2) ENSP00000502597.1:n.-41+65C>A
ENST00000676411.1:c.-40-683C>A (CCND2) ENSP00000502654.1:n.-40-683C>A
NR_125790.1:n.126+2741G>T (CCND2-AS1)
NR_149145.1:n.182+1978G>T (CCND2-AS1)
NR_149146.1:n.182+1978G>T (CCND2-AS1)