Canonical Allele Identifier: CA383661496
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2120513185

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4274072T>C , CM000674.2:g.4274072T>C GRCh38
NC_000012.11:g.4383238T>C , CM000674.1:g.4383238T>C GRCh37
NC_000012.10:g.4253499T>C NCBI36
NG_034254.1:g.5337T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.32T>C (CCND2) MANE Select ENSP00000261254.3:p.Val11Ala
ENST00000536537.2:n.311T>C (CCND2)
ENST00000648100.1:c.32T>C ENSP00000497536.1:p.Val11Ala
ENST00000674624.1:c.32T>C ENSP00000501898.1:p.Val11Ala
ENST00000675880.1:c.32T>C (CCND2) ENSP00000502508.1:p.Val11Ala
ENST00000676279.1:c.32T>C (CCND2) ENSP00000502597.1:p.Val11Ala
ENST00000676411.1:c.32T>C (CCND2) ENSP00000502654.1:p.Val11Ala
ENST00000261254.7:c.32T>C (CCND2) ENSP00000261254.3:p.Val11Ala
NM_001759.3:c.32T>C (CCND2) NP_001750.1:p.Val11Ala
NR_125790.1:n.126+1987A>G (CCND2-AS1)
XM_005253813.3:c.32T>C (CCND2) XP_005253870.1:p.Val11Ala
NR_149145.1:n.182+1224A>G (CCND2-AS1)
NR_149146.1:n.182+1224A>G (CCND2-AS1)
NM_001759.4:c.32T>C (CCND2) MANE Select NP_001750.1:p.Val11Ala