Canonical Allele Identifier: CA2617153798

Gene: CCND2 CCND2-AS1

Linked Data

• gnomAD v4: 12-4273748-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4273748T>C , CM000674.2:g.4273748T>C	GRCh38
NC_000012.11:g.4382914T>C , CM000674.1:g.4382914T>C	GRCh37
NC_000012.10:g.4253175T>C	NCBI36
NG_034254.1:g.5013T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676279.1:c.-40-253T>C (CCND2)	ENSP00000502597.1:n.-40-253T>C
ENST00000676411.1:c.-40-253T>C (CCND2)	ENSP00000502654.1:n.-40-253T>C
NM_001759.3:c.-293T>C (CCND2)	NP_001750.1:n.-293T>C
NR_125790.1:n.126+2311A>G (CCND2-AS1)
XM_005253813.3:c.-293T>C (CCND2)	XP_005253870.1:n.-293T>C
NR_149145.1:n.182+1548A>G (CCND2-AS1)
NR_149146.1:n.182+1548A>G (CCND2-AS1)