Canonical Allele Identifier: CA2617153817

Gene: CCND2 CCND2-AS1

Linked Data

• gnomAD v4: 12-4273753-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273753C>A , CM000674.2:g.4273753C>A	GRCh38
NC_000012.11:g.4382919C>A , CM000674.1:g.4382919C>A	GRCh37
NC_000012.10:g.4253180C>A	NCBI36
NG_034254.1:g.5018C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676279.1:c.-40-248C>A (CCND2)	ENSP00000502597.1:n.-40-248C>A
ENST00000676411.1:c.-40-248C>A (CCND2)	ENSP00000502654.1:n.-40-248C>A
NM_001759.3:c.-288C>A (CCND2)	NP_001750.1:n.-288C>A
NR_125790.1:n.126+2306G>T (CCND2-AS1)
XM_005253813.3:c.-288C>A (CCND2)	XP_005253870.1:n.-288C>A
NR_149145.1:n.182+1543G>T (CCND2-AS1)
NR_149146.1:n.182+1543G>T (CCND2-AS1)