Canonical Allele Identifier: CA2617153347
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273639_4273691del , CM000674.2:g.4273639_4273691del GRCh38
NC_000012.11:g.4382805_4382857del , CM000674.1:g.4382805_4382857del GRCh37
NC_000012.10:g.4253066_4253118del NCBI36
NG_034254.1:g.4904_4956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-362_-40-310del (CCND2) ENSP00000502597.1:n.-40-362_-40-310del
ENST00000676411.1:c.-40-362_-40-310del (CCND2) ENSP00000502654.1:n.-40-362_-40-310del
NR_125790.1:n.126+2374_126+2426del (CCND2-AS1)
NR_149145.1:n.182+1611_182+1663del (CCND2-AS1)
NR_149146.1:n.182+1611_182+1663del (CCND2-AS1)