Canonical Allele Identifier: CA2013084022

Gene: CCND2 CCND2-AS1

Linked Data

• dbSNP Id: rs1863809705

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273351_4273353dup , CM000674.2:g.4273351_4273353dup	GRCh38
NC_000012.11:g.4382517_4382519dup , CM000674.1:g.4382517_4382519dup	GRCh37
NC_000012.10:g.4252778_4252780dup	NCBI36
NG_034254.1:g.4616_4618dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676279.1:c.-41+98_-41+100dup (CCND2)	ENSP00000502597.1:n.-41+98_-41+100dup
ENST00000676411.1:c.-40-650_-40-648dup (CCND2)	ENSP00000502654.1:n.-40-650_-40-648dup
NR_125790.1:n.126+2706_126+2708dup (CCND2-AS1)
NR_149145.1:n.182+1943_182+1945dup (CCND2-AS1)
NR_149146.1:n.182+1943_182+1945dup (CCND2-AS1)