Canonical Allele Identifier: CA944205308

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4288825C>T , CM000674.2:g.4288825C>T	GRCh38
NC_000012.11:g.4397991C>T , CM000674.1:g.4397991C>T	GRCh37
NC_000012.10:g.4268252C>T	NCBI36
NG_034254.1:g.20090C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001759.4:c.572-17C>T MANE Select	NP_001750.1:n.572-17C>T
ENST00000261254.8:c.572-17C>T MANE Select	ENSP00000261254.3:n.572-17C>T
NM_001759.3:c.572-17C>T	NP_001750.1:n.572-17C>T
ENST00000261254.7:c.572-17C>T	ENSP00000261254.3:n.572-17C>T
ENST00000536537.1:c.318-8932C>T
ENST00000536537.2:n.851-8932C>T
ENST00000536795.1:n.253-17C>T
ENST00000648100.1:c.572-17C>T	ENSP00000497536.1:n.572-17C>T
ENST00000674624.1:c.572-17C>T	ENSP00000501898.1:n.572-17C>T
ENST00000675468.1:n.496-17C>T
ENST00000675880.1:c.614-17C>T	ENSP00000502508.1:n.614-17C>T
ENST00000676279.1:c.572-17C>T	ENSP00000502597.1:n.572-17C>T
ENST00000676411.1:c.572-17C>T	ENSP00000502654.1:n.572-17C>T