Canonical Allele Identifier: CA2013084272
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863817247
gnomAD v4: 12-4273761-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273761C>T , CM000674.2:g.4273761C>T GRCh38
NC_000012.11:g.4382927C>T , CM000674.1:g.4382927C>T GRCh37
NC_000012.10:g.4253188C>T NCBI36
NG_034254.1:g.5026C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-240C>T (CCND2) ENSP00000502597.1:n.-40-240C>T
ENST00000676411.1:c.-40-240C>T (CCND2) ENSP00000502654.1:n.-40-240C>T
NM_001759.3:c.-280C>T (CCND2) NP_001750.1:n.-280C>T
NR_125790.1:n.126+2298G>A (CCND2-AS1)
XM_005253813.3:c.-280C>T (CCND2) XP_005253870.1:n.-280C>T
NR_149145.1:n.182+1535G>A (CCND2-AS1)
NR_149146.1:n.182+1535G>A (CCND2-AS1)