Canonical Allele Identifier: CA232171379
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs968990207
MyVariant Identifiers: chr12:g.4382589G>T (hg19) chr12:g.4273423G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273423G>T , CM000674.2:g.4273423G>T GRCh38
NC_000012.11:g.4382589G>T , CM000674.1:g.4382589G>T GRCh37
NC_000012.10:g.4252850G>T NCBI36
NG_034254.1:g.4688G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+170G>T (CCND2) ENSP00000502597.1:n.-41+170G>T
ENST00000676411.1:c.-40-578G>T (CCND2) ENSP00000502654.1:n.-40-578G>T
NR_125790.1:n.126+2636C>A (CCND2-AS1)
NR_149145.1:n.182+1873C>A (CCND2-AS1)
NR_149146.1:n.182+1873C>A (CCND2-AS1)
Search 100 bp 5'
Search 100 bp 3'