Canonical Allele Identifier: CA6395323

Gene: CCND2

Linked Data

• ClinVar Variation Id: 511836
• ClinVar RCV Id: RCV001697947 ; RCV002483691 ; RCV003927992
• dbSNP Id: rs145050894
• ExAC: 12:4409061 G / A
• gnomAD v2: 12-4409061-G-A
• gnomAD v3: 12-4299895-G-A
• gnomAD v4: 12-4299895-G-A
• MyVariant Identifiers: chr12:g.4409061G>A (hg19) ; chr12:g.4299895G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4299895G>A , CM000674.2:g.4299895G>A	GRCh38
NC_000012.11:g.4409061G>A , CM000674.1:g.4409061G>A	GRCh37
NC_000012.10:g.4279322G>A	NCBI36
NG_034254.1:g.31160G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.756G>A MANE Select	ENSP00000261254.3:p.Ala252=
ENST00000648100.1:c.720+10905G>A	ENSP00000497536.1:n.720+10905G>A
ENST00000674624.1:c.720+10905G>A	ENSP00000501898.1:n.720+10905G>A
ENST00000675468.1:n.680G>A
ENST00000675880.1:c.798G>A	ENSP00000502508.1:p.Ala266=
ENST00000676279.1:c.756G>A	ENSP00000502597.1:p.Ala252=
ENST00000676411.1:c.756G>A	ENSP00000502654.1:p.Ala252=
ENST00000261254.7:c.756G>A	ENSP00000261254.3:p.Ala252=
NM_001759.3:c.756G>A	NP_001750.1:p.Ala252=
NM_001759.4:c.756G>A MANE Select	NP_001750.1:p.Ala252=