Canonical Allele Identifier: CA2013084004
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273313T= , CM000674.2:g.4273313T= GRCh38
NC_000012.11:g.4382479T= , CM000674.1:g.4382479T= GRCh37
NC_000012.10:g.4252740T= NCBI36
NG_034254.1:g.4578T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+60T= (CCND2) ENSP00000502597.1:n.-41+60T=
ENST00000676411.1:c.-40-688T= (CCND2) ENSP00000502654.1:n.-40-688T=
NR_125790.1:n.126+2746A= (CCND2-AS1)
NR_149145.1:n.182+1983A= (CCND2-AS1)
NR_149146.1:n.182+1983A= (CCND2-AS1)
Search 100 bp 5'
Search 100 bp 3'