Canonical Allele Identifier: CA688960356

Gene: CCND2 CCND2-AS1

Linked Data

• dbSNP Id: rs1157013054
• gnomAD v3: 12-4273372-C-CG
• gnomAD v4: 12-4273372-C-CG
• MyVariant Identifiers: chr12:g.4382538_4382539insG (hg19) ; chr12:g.4273372_4273373insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273372_4273373insG , CM000674.2:g.4273372_4273373insG	GRCh38
NC_000012.11:g.4382538_4382539insG , CM000674.1:g.4382538_4382539insG	GRCh37
NC_000012.10:g.4252799_4252800insG	NCBI36
NG_034254.1:g.4637_4638insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676279.1:c.-41+119_-41+120insG (CCND2)	ENSP00000502597.1:n.-41+119_-41+120insG
ENST00000676411.1:c.-40-629_-40-628insG (CCND2)	ENSP00000502654.1:n.-40-629_-40-628insG
NR_125790.1:n.126+2686_126+2687insC (CCND2-AS1)
NR_149145.1:n.182+1923_182+1924insC (CCND2-AS1)
NR_149146.1:n.182+1923_182+1924insC (CCND2-AS1)