Canonical Allele Identifier: CA944199214
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863815214

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273669_4273682del , CM000674.2:g.4273669_4273682del GRCh38
NC_000012.11:g.4382835_4382848del , CM000674.1:g.4382835_4382848del GRCh37
NC_000012.10:g.4253096_4253109del NCBI36
NG_034254.1:g.4934_4947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-332_-40-319del (CCND2) ENSP00000502597.1:n.-40-332_-40-319del
ENST00000676411.1:c.-40-332_-40-319del (CCND2) ENSP00000502654.1:n.-40-332_-40-319del
NR_125790.1:n.126+2388_126+2401del (CCND2-AS1)
NR_149145.1:n.182+1625_182+1638del (CCND2-AS1)
NR_149146.1:n.182+1625_182+1638del (CCND2-AS1)