Canonical Allele Identifier: CA2617153678
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273721_4273789del , CM000674.2:g.4273721_4273789del GRCh38
NC_000012.11:g.4382887_4382955del , CM000674.1:g.4382887_4382955del GRCh37
NC_000012.10:g.4253148_4253216del NCBI36
NG_034254.1:g.4986_5054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-280_-40-212del (CCND2) ENSP00000502597.1:n.-40-280_-40-212del
ENST00000676411.1:c.-40-280_-40-212del (CCND2) ENSP00000502654.1:n.-40-280_-40-212del
NR_125790.1:n.126+2278_126+2346del (CCND2-AS1)
NR_149145.1:n.182+1515_182+1583del (CCND2-AS1)
NR_149146.1:n.182+1515_182+1583del (CCND2-AS1)