Canonical Allele Identifier: CA232171406
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1004201749
MyVariant Identifiers: chr12:g.4382708_4382711del (hg19) chr12:g.4273542_4273545del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273546_4273549del , CM000674.2:g.4273546_4273549del GRCh38
NC_000012.11:g.4382712_4382715del , CM000674.1:g.4382712_4382715del GRCh37
NC_000012.10:g.4252973_4252976del NCBI36
NG_034254.1:g.4811_4814del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+293_-41+296del (CCND2) ENSP00000502597.1:n.-41+293_-41+296del
ENST00000676411.1:c.-40-455_-40-452del (CCND2) ENSP00000502654.1:n.-40-455_-40-452del
NR_125790.1:n.126+2514_126+2517del (CCND2-AS1)
NR_149145.1:n.182+1751_182+1754del (CCND2-AS1)
NR_149146.1:n.182+1751_182+1754del (CCND2-AS1)
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