Canonical Allele Identifier: CA231743963

Gene: CCND2

Linked Data

• dbSNP Id: rs964191473
• gnomAD v2: 12-4405310-C-A
• gnomAD v3: 12-4296144-C-A
• gnomAD v4: 12-4296144-C-A
• MyVariant Identifiers: chr12:g.4405310C>A (hg19) ; chr12:g.4296144C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4296144C>A , CM000674.2:g.4296144C>A	GRCh38
NC_000012.11:g.4405310C>A , CM000674.1:g.4405310C>A	GRCh37
NC_000012.10:g.4275571C>A	NCBI36
NG_034254.1:g.27409C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261254.8:c.721-3716C>A MANE Select	ENSP00000261254.3:n.721-3716C>A
ENST00000536537.2:n.851-1613C>A
ENST00000648100.1:c.720+7154C>A	ENSP00000497536.1:n.720+7154C>A
ENST00000674624.1:c.720+7154C>A	ENSP00000501898.1:n.720+7154C>A
ENST00000675468.1:n.645-3716C>A
ENST00000675880.1:c.763-3716C>A	ENSP00000502508.1:n.763-3716C>A
ENST00000676279.1:c.721-3716C>A	ENSP00000502597.1:n.721-3716C>A
ENST00000676411.1:c.721-3716C>A	ENSP00000502654.1:n.721-3716C>A
ENST00000261254.7:c.721-3716C>A	ENSP00000261254.3:n.721-3716C>A
ENST00000536537.1:c.318-1613C>A
NM_001759.3:c.721-3716C>A	NP_001750.1:n.721-3716C>A
NM_001759.4:c.721-3716C>A MANE Select	NP_001750.1:n.721-3716C>A