Canonical Allele Identifier: CA602788657

Gene: CCND2

Linked Data

• dbSNP Id: rs377071471
• gnomAD v2: 12-4405292-A-C
• gnomAD v3: 12-4296126-A-C
• gnomAD v4: 12-4296126-A-C
• MyVariant Identifiers: chr12:g.4405292A>C (hg19) ; chr12:g.4296126A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4296126A>C , CM000674.2:g.4296126A>C	GRCh38
NC_000012.11:g.4405292A>C , CM000674.1:g.4405292A>C	GRCh37
NC_000012.10:g.4275553A>C	NCBI36
NG_034254.1:g.27391A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.721-3734A>C MANE Select	ENSP00000261254.3:n.721-3734A>C
ENST00000536537.2:n.851-1631A>C
ENST00000648100.1:c.720+7136A>C	ENSP00000497536.1:n.720+7136A>C
ENST00000674624.1:c.720+7136A>C	ENSP00000501898.1:n.720+7136A>C
ENST00000675468.1:n.645-3734A>C
ENST00000675880.1:c.763-3734A>C	ENSP00000502508.1:n.763-3734A>C
ENST00000676279.1:c.721-3734A>C	ENSP00000502597.1:n.721-3734A>C
ENST00000676411.1:c.721-3734A>C	ENSP00000502654.1:n.721-3734A>C
ENST00000261254.7:c.721-3734A>C	ENSP00000261254.3:n.721-3734A>C
ENST00000536537.1:c.318-1631A>C
NM_001759.3:c.721-3734A>C	NP_001750.1:n.721-3734A>C
NM_001759.4:c.721-3734A>C MANE Select	NP_001750.1:n.721-3734A>C