Canonical Allele Identifier: CA688960329

Gene: CCND2 CCND2-AS1

Linked Data

• dbSNP Id: rs1318255129
• gnomAD v3: 12-4273323-TTGTC-T
• gnomAD v4: 12-4273323-TTGTC-T
• MyVariant Identifiers: chr12:g.4382490_4382493del (hg19) ; chr12:g.4273324_4273327del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273326_4273329del , CM000674.2:g.4273326_4273329del	GRCh38
NC_000012.11:g.4382492_4382495del , CM000674.1:g.4382492_4382495del	GRCh37
NC_000012.10:g.4252753_4252756del	NCBI36
NG_034254.1:g.4591_4594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676279.1:c.-41+73_-41+76del (CCND2)	ENSP00000502597.1:n.-41+73_-41+76del
ENST00000676411.1:c.-40-675_-40-672del (CCND2)	ENSP00000502654.1:n.-40-675_-40-672del
NR_125790.1:n.126+2732_126+2735del (CCND2-AS1)
NR_149145.1:n.182+1969_182+1972del (CCND2-AS1)
NR_149146.1:n.182+1969_182+1972del (CCND2-AS1)