Canonical Allele Identifier: CA688960327
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1254867593
gnomAD v3: 12-4273309-G-T
gnomAD v4: 12-4273309-G-T
MyVariant Identifiers: chr12:g.4382475G>T (hg19) chr12:g.4273309G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273309G>T , CM000674.2:g.4273309G>T GRCh38
NC_000012.11:g.4382475G>T , CM000674.1:g.4382475G>T GRCh37
NC_000012.10:g.4252736G>T NCBI36
NG_034254.1:g.4574G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+56G>T (CCND2) ENSP00000502597.1:n.-41+56G>T
ENST00000676411.1:c.-40-692G>T (CCND2) ENSP00000502654.1:n.-40-692G>T
NR_125790.1:n.126+2750C>A (CCND2-AS1)
NR_149145.1:n.182+1987C>A (CCND2-AS1)
NR_149146.1:n.182+1987C>A (CCND2-AS1)
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