Canonical Allele Identifier: CA6395259

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4278918C>G , CM000674.2:g.4278918C>G	GRCh38
NC_000012.11:g.4388084C>G , CM000674.1:g.4388084C>G	GRCh37
NC_000012.10:g.4258345C>G	NCBI36
NG_034254.1:g.10183C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.570C>G MANE Select	ENSP00000261254.3:p.Thr190=
ENST00000536537.2:n.849C>G
ENST00000648100.1:c.570C>G	ENSP00000497536.1:p.Thr190=
ENST00000674624.1:c.570C>G	ENSP00000501898.1:p.Thr190=
ENST00000675468.1:n.494C>G
ENST00000675880.1:c.570C>G	ENSP00000502508.1:p.Thr190=
ENST00000676279.1:c.570C>G	ENSP00000502597.1:p.Thr190=
ENST00000676411.1:c.570C>G	ENSP00000502654.1:p.Thr190=
ENST00000261254.7:c.570C>G	ENSP00000261254.3:p.Thr190=
ENST00000536537.1:c.316C>G
ENST00000536795.1:n.251C>G
ENST00000541542.1:n.119C>G
NM_001759.3:c.570C>G	NP_001750.1:p.Thr190=
XM_005253813.3:c.570C>G	XP_005253870.1:p.Thr190=
NM_001759.4:c.570C>G MANE Select	NP_001750.1:p.Thr190=