Canonical Allele Identifier: CA2617153336
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273640_4273677del , CM000674.2:g.4273640_4273677del GRCh38
NC_000012.11:g.4382806_4382843del , CM000674.1:g.4382806_4382843del GRCh37
NC_000012.10:g.4253067_4253104del NCBI36
NG_034254.1:g.4905_4942del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-361_-40-324del (CCND2) ENSP00000502597.1:n.-40-361_-40-324del
ENST00000676411.1:c.-40-361_-40-324del (CCND2) ENSP00000502654.1:n.-40-361_-40-324del
NR_125790.1:n.126+2389_126+2426del (CCND2-AS1)
NR_149145.1:n.182+1626_182+1663del (CCND2-AS1)
NR_149146.1:n.182+1626_182+1663del (CCND2-AS1)