Canonical Allele Identifier: CA478054290
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

gnomAD v4: 12-4274121-G-T
MyVariant Identifiers: chr12:g.4383287G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4274121G>T , CM000674.2:g.4274121G>T GRCh38
NC_000012.11:g.4383287G>T , CM000674.1:g.4383287G>T GRCh37
NC_000012.10:g.4253548G>T NCBI36
NG_034254.1:g.5386G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261254.8:c.81G>T (CCND2) MANE Select ENSP00000261254.3:p.Leu27=
ENST00000536537.2:n.360G>T (CCND2)
ENST00000648100.1:c.81G>T ENSP00000497536.1:p.Leu27=
ENST00000674624.1:c.81G>T ENSP00000501898.1:p.Leu27=
ENST00000675880.1:c.81G>T (CCND2) ENSP00000502508.1:p.Leu27=
ENST00000676279.1:c.81G>T (CCND2) ENSP00000502597.1:p.Leu27=
ENST00000676411.1:c.81G>T (CCND2) ENSP00000502654.1:p.Leu27=
ENST00000261254.7:c.81G>T (CCND2) ENSP00000261254.3:p.Leu27=
NM_001759.3:c.81G>T (CCND2) NP_001750.1:p.Leu27=
NR_125790.1:n.126+1938C>A (CCND2-AS1)
XM_005253813.3:c.81G>T (CCND2) XP_005253870.1:p.Leu27=
NR_149145.1:n.182+1175C>A (CCND2-AS1)
NR_149146.1:n.182+1175C>A (CCND2-AS1)
NM_001759.4:c.81G>T (CCND2) MANE Select NP_001750.1:p.Leu27=
Search 100 bp 5'
Search 100 bp 3'