Canonical Allele Identifier: CA232171482

Gene: CCND2 CCND2-AS1

Linked Data

• dbSNP Id: rs904796145
• MyVariant Identifiers: chr12:g.4382948G>A (hg19) ; chr12:g.4273782G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273782G>A , CM000674.2:g.4273782G>A	GRCh38
NC_000012.11:g.4382948G>A , CM000674.1:g.4382948G>A	GRCh37
NC_000012.10:g.4253209G>A	NCBI36
NG_034254.1:g.5047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.-259G>A (CCND2) MANE Select	ENSP00000261254.3:n.-259G>A
ENST00000536537.2:n.21G>A (CCND2)
ENST00000648100.1:c.-259G>A	ENSP00000497536.1:n.-259G>A
ENST00000674624.1:c.-259G>A	ENSP00000501898.1:n.-259G>A
ENST00000675880.1:c.-259G>A (CCND2)	ENSP00000502508.1:n.-259G>A
ENST00000676279.1:c.-40-219G>A (CCND2)	ENSP00000502597.1:n.-40-219G>A
ENST00000676411.1:c.-40-219G>A (CCND2)	ENSP00000502654.1:n.-40-219G>A
ENST00000261254.7:c.-259G>A (CCND2)	ENSP00000261254.3:n.-259G>A
NM_001759.3:c.-259G>A (CCND2)	NP_001750.1:n.-259G>A
NR_125790.1:n.126+2277C>T (CCND2-AS1)
XM_005253813.3:c.-259G>A (CCND2)	XP_005253870.1:n.-259G>A
NR_149145.1:n.182+1514C>T (CCND2-AS1)
NR_149146.1:n.182+1514C>T (CCND2-AS1)
NM_001759.4:c.-259G>A (CCND2) MANE Select	NP_001750.1:n.-259G>A