Canonical Allele Identifier: CA2013086903

Gene: CCND2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4279105C>A , CM000674.2:g.4279105C>A	GRCh38
NC_000012.11:g.4388271C>A , CM000674.1:g.4388271C>A	GRCh37
NC_000012.10:g.4258532C>A	NCBI36
NG_034254.1:g.10370C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.571+186C>A MANE Select	ENSP00000261254.3:n.571+186C>A
ENST00000536537.2:n.850+186C>A
ENST00000648100.1:c.571+186C>A	ENSP00000497536.1:n.571+186C>A
ENST00000674624.1:c.571+186C>A	ENSP00000501898.1:n.571+186C>A
ENST00000675468.1:n.495+186C>A
ENST00000675880.1:c.571+186C>A	ENSP00000502508.1:n.571+186C>A
ENST00000676279.1:c.571+186C>A	ENSP00000502597.1:n.571+186C>A
ENST00000676411.1:c.571+186C>A	ENSP00000502654.1:n.571+186C>A
ENST00000261254.7:c.571+186C>A	ENSP00000261254.3:n.571+186C>A
ENST00000536537.1:c.317+186C>A
ENST00000536795.1:n.252+186C>A
ENST00000541542.1:n.120+186C>A
NM_001759.3:c.571+186C>A	NP_001750.1:n.571+186C>A
XM_005253813.3:c.571+186C>A	XP_005253870.1:n.571+186C>A
NM_001759.4:c.571+186C>A MANE Select	NP_001750.1:n.571+186C>A