Canonical Allele Identifier: CA2617153416
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273663_4273694del , CM000674.2:g.4273663_4273694del GRCh38
NC_000012.11:g.4382829_4382860del , CM000674.1:g.4382829_4382860del GRCh37
NC_000012.10:g.4253090_4253121del NCBI36
NG_034254.1:g.4928_4959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-338_-40-307del (CCND2) ENSP00000502597.1:n.-40-338_-40-307del
ENST00000676411.1:c.-40-338_-40-307del (CCND2) ENSP00000502654.1:n.-40-338_-40-307del
NR_125790.1:n.126+2373_126+2404del (CCND2-AS1)
NR_149145.1:n.182+1610_182+1641del (CCND2-AS1)
NR_149146.1:n.182+1610_182+1641del (CCND2-AS1)