Canonical Allele Identifier: CA383661725

Gene: CCND2 CCND2-AS1

Linked Data

• dbSNP Id: rs1449067414
• gnomAD v4: 12-4274179-G-A
• MyVariant Identifiers: chr12:g.4383345G>A (hg19) ; chr12:g.4274179G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4274179G>A , CM000674.2:g.4274179G>A	GRCh38
NC_000012.11:g.4383345G>A , CM000674.1:g.4383345G>A	GRCh37
NC_000012.10:g.4253606G>A	NCBI36
NG_034254.1:g.5444G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261254.8:c.139G>A (CCND2) MANE Select	ENSP00000261254.3:p.Val47Met
ENST00000536537.2:n.418G>A (CCND2)
ENST00000648100.1:c.139G>A	ENSP00000497536.1:p.Val47Met
ENST00000674624.1:c.139G>A	ENSP00000501898.1:p.Val47Met
ENST00000675880.1:c.139G>A (CCND2)	ENSP00000502508.1:p.Val47Met
ENST00000676279.1:c.139G>A (CCND2)	ENSP00000502597.1:p.Val47Met
ENST00000676411.1:c.139G>A (CCND2)	ENSP00000502654.1:p.Val47Met
ENST00000261254.7:c.139G>A (CCND2)	ENSP00000261254.3:p.Val47Met
NM_001759.3:c.139G>A (CCND2)	NP_001750.1:p.Val47Met
NR_125790.1:n.126+1880C>T (CCND2-AS1)
XM_005253813.3:c.139G>A (CCND2)	XP_005253870.1:p.Val47Met
NR_149145.1:n.182+1117C>T (CCND2-AS1)
NR_149146.1:n.182+1117C>T (CCND2-AS1)
NM_001759.4:c.139G>A (CCND2) MANE Select	NP_001750.1:p.Val47Met