Canonical Allele Identifier: CA944199073
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1863809934
gnomAD v3: 12-4273366-C-T
gnomAD v4: 12-4273366-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273366C>T , CM000674.2:g.4273366C>T GRCh38
NC_000012.11:g.4382532C>T , CM000674.1:g.4382532C>T GRCh37
NC_000012.10:g.4252793C>T NCBI36
NG_034254.1:g.4631C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+113C>T (CCND2) ENSP00000502597.1:n.-41+113C>T
ENST00000676411.1:c.-40-635C>T (CCND2) ENSP00000502654.1:n.-40-635C>T
NR_125790.1:n.126+2693G>A (CCND2-AS1)
NR_149145.1:n.182+1930G>A (CCND2-AS1)
NR_149146.1:n.182+1930G>A (CCND2-AS1)
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