Canonical Allele Identifier: CA688960414
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs924618175
gnomAD v3: 12-4273469-A-C
gnomAD v4: 12-4273469-A-C
MyVariant Identifiers: chr12:g.4382635A>C (hg19) chr12:g.4273469A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273469A>C , CM000674.2:g.4273469A>C GRCh38
NC_000012.11:g.4382635A>C , CM000674.1:g.4382635A>C GRCh37
NC_000012.10:g.4252896A>C NCBI36
NG_034254.1:g.4734A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-41+216A>C (CCND2) ENSP00000502597.1:n.-41+216A>C
ENST00000676411.1:c.-40-532A>C (CCND2) ENSP00000502654.1:n.-40-532A>C
NR_125790.1:n.126+2590T>G (CCND2-AS1)
NR_149145.1:n.182+1827T>G (CCND2-AS1)
NR_149146.1:n.182+1827T>G (CCND2-AS1)
Search 100 bp 5'
Search 100 bp 3'