Canonical Allele Identifier: CA477949903

Gene: CCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4288864A>G , CM000674.2:g.4288864A>G	GRCh38
NC_000012.11:g.4398030A>G , CM000674.1:g.4398030A>G	GRCh37
NC_000012.10:g.4268291A>G	NCBI36
NG_034254.1:g.20129A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.594A>G MANE Select	ENSP00000261254.3:p.Pro198=
ENST00000536537.2:n.851-8893A>G
ENST00000648100.1:c.594A>G	ENSP00000497536.1:p.Pro198=
ENST00000674624.1:c.594A>G	ENSP00000501898.1:p.Pro198=
ENST00000675468.1:n.518A>G
ENST00000675880.1:c.636A>G	ENSP00000502508.1:p.Pro212=
ENST00000676279.1:c.594A>G	ENSP00000502597.1:p.Pro198=
ENST00000676411.1:c.594A>G	ENSP00000502654.1:p.Pro198=
ENST00000261254.7:c.594A>G	ENSP00000261254.3:p.Pro198=
ENST00000536537.1:c.318-8893A>G
ENST00000536795.1:n.275A>G
NM_001759.3:c.594A>G	NP_001750.1:p.Pro198=
NM_001759.4:c.594A>G MANE Select	NP_001750.1:p.Pro198=