Canonical Allele Identifier: CA688960359
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1185227875
gnomAD v3: 12-4273384-G-T
gnomAD v4: 12-4273384-G-T
MyVariant Identifiers: chr12:g.4382550G>T (hg19) chr12:g.4273384G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273384G>T , CM000674.2:g.4273384G>T GRCh38
NC_000012.11:g.4382550G>T , CM000674.1:g.4382550G>T GRCh37
NC_000012.10:g.4252811G>T NCBI36
NG_034254.1:g.4649G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+131G>T (CCND2) ENSP00000502597.1:n.-41+131G>T
ENST00000676411.1:c.-40-617G>T (CCND2) ENSP00000502654.1:n.-40-617G>T
NR_125790.1:n.126+2675C>A (CCND2-AS1)
NR_149145.1:n.182+1912C>A (CCND2-AS1)
NR_149146.1:n.182+1912C>A (CCND2-AS1)
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