Canonical Allele Identifier: CA2617153434
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273669_4273692del , CM000674.2:g.4273669_4273692del GRCh38
NC_000012.11:g.4382835_4382858del , CM000674.1:g.4382835_4382858del GRCh37
NC_000012.10:g.4253096_4253119del NCBI36
NG_034254.1:g.4934_4957del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-332_-40-309del (CCND2) ENSP00000502597.1:n.-40-332_-40-309del
ENST00000676411.1:c.-40-332_-40-309del (CCND2) ENSP00000502654.1:n.-40-332_-40-309del
NR_125790.1:n.126+2376_126+2399del (CCND2-AS1)
NR_149145.1:n.182+1613_182+1636del (CCND2-AS1)
NR_149146.1:n.182+1613_182+1636del (CCND2-AS1)