Canonical Allele Identifier: CA2617153637
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273701_4273703del , CM000674.2:g.4273701_4273703del GRCh38
NC_000012.11:g.4382867_4382869del , CM000674.1:g.4382867_4382869del GRCh37
NC_000012.10:g.4253128_4253130del NCBI36
NG_034254.1:g.4966_4968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-300_-40-298del (CCND2) ENSP00000502597.1:n.-40-300_-40-298del
ENST00000676411.1:c.-40-300_-40-298del (CCND2) ENSP00000502654.1:n.-40-300_-40-298del
NR_125790.1:n.126+2356_126+2358del (CCND2-AS1)
NR_149145.1:n.182+1593_182+1595del (CCND2-AS1)
NR_149146.1:n.182+1593_182+1595del (CCND2-AS1)