Canonical Allele Identifier: CA15759938
Gene: CCND2 HGNC NCBI
MyVariant.info:
GRCh38 chr12:g.4279105C>T
GRCh37 chr12:g.4388271C>T
gnomAD v2:
12:4388271 C / T
gnomAD v3:
12:4279105 C / T
gnomAD v4:
chr12-4279105-C-T
Joint Max Group AF 0.12214038 (NFE)
Genomes Max Group AF 0.12214038 (NFE)
ClinVar RCV:
RCV001595234
ClinVar Variation:
1220672
dbSNP:
3217810
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4279105C>T , CM000674.2:g.4279105C>T GRCh38
NC_000012.11:g.4388271C>T , CM000674.1:g.4388271C>T GRCh37
NC_000012.10:g.4258532C>T NCBI36
NG_034254.1:g.10370C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.571+186C>T MANE Select ENSP00000261254.3:n.571+186C>T
ENST00000536537.2:n.850+186C>T
ENST00000648100.1:c.571+186C>T ENSP00000497536.1:n.571+186C>T
ENST00000674624.1:c.571+186C>T ENSP00000501898.1:n.571+186C>T
ENST00000675468.1:n.495+186C>T
ENST00000675880.1:c.571+186C>T ENSP00000502508.1:n.571+186C>T
ENST00000676279.1:c.571+186C>T ENSP00000502597.1:n.571+186C>T
ENST00000676411.1:c.571+186C>T ENSP00000502654.1:n.571+186C>T
ENST00000261254.7:c.571+186C>T ENSP00000261254.3:n.571+186C>T
ENST00000536537.1:c.317+186C>T
ENST00000536795.1:n.252+186C>T
ENST00000541542.1:n.120+186C>T
NM_001759.3:c.571+186C>T NP_001750.1:n.571+186C>T
XM_005253813.3:c.571+186C>T XP_005253870.1:n.571+186C>T
NM_001759.4:c.571+186C>T MANE Select NP_001750.1:n.571+186C>T
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