Canonical Allele Identifier: CA231743961

Gene: CCND2

Linked Data

• dbSNP Id: rs1007974891
• gnomAD v3: 12-4296138-C-T
• gnomAD v4: 12-4296138-C-T
• MyVariant Identifiers: chr12:g.4405304C>T (hg19) ; chr12:g.4296138C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4296138C>T , CM000674.2:g.4296138C>T	GRCh38
NC_000012.11:g.4405304C>T , CM000674.1:g.4405304C>T	GRCh37
NC_000012.10:g.4275565C>T	NCBI36
NG_034254.1:g.27403C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.721-3722C>T MANE Select	ENSP00000261254.3:n.721-3722C>T
ENST00000536537.2:n.851-1619C>T
ENST00000648100.1:c.720+7148C>T	ENSP00000497536.1:n.720+7148C>T
ENST00000674624.1:c.720+7148C>T	ENSP00000501898.1:n.720+7148C>T
ENST00000675468.1:n.645-3722C>T
ENST00000675880.1:c.763-3722C>T	ENSP00000502508.1:n.763-3722C>T
ENST00000676279.1:c.721-3722C>T	ENSP00000502597.1:n.721-3722C>T
ENST00000676411.1:c.721-3722C>T	ENSP00000502654.1:n.721-3722C>T
ENST00000261254.7:c.721-3722C>T	ENSP00000261254.3:n.721-3722C>T
ENST00000536537.1:c.318-1619C>T
NM_001759.3:c.721-3722C>T	NP_001750.1:n.721-3722C>T
NM_001759.4:c.721-3722C>T MANE Select	NP_001750.1:n.721-3722C>T