Canonical Allele Identifier: CA2617153538
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273681_4273729del , CM000674.2:g.4273681_4273729del GRCh38
NC_000012.11:g.4382847_4382895del , CM000674.1:g.4382847_4382895del GRCh37
NC_000012.10:g.4253108_4253156del NCBI36
NG_034254.1:g.4946_4994del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-320_-40-272del (CCND2) ENSP00000502597.1:n.-40-320_-40-272del
ENST00000676411.1:c.-40-320_-40-272del (CCND2) ENSP00000502654.1:n.-40-320_-40-272del
NR_125790.1:n.126+2333_126+2381del (CCND2-AS1)
NR_149145.1:n.182+1570_182+1618del (CCND2-AS1)
NR_149146.1:n.182+1570_182+1618del (CCND2-AS1)