Canonical Allele Identifier: CA13444079
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs3212891

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69650739C>A , CM000673.2:g.69650739C>A GRCh38
NC_000011.9:g.69465507C>A , CM000673.1:g.69465507C>A GRCh37
NC_000011.8:g.69174688C>A NCBI36
NG_007375.1:g.14635C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.724-379C>A MANE Select ENSP00000227507.2:n.724-379C>A
ENST00000227507.2:c.724-379C>A ENSP00000227507.2:n.724-379C>A
ENST00000542367.1:n.187-379C>A
NM_053056.2:c.724-379C>A NP_444284.1:n.724-379C>A
XM_006718653.2:c.748-379C>A XP_006718716.1:n.748-379C>A
NM_053056.3:c.724-379C>A MANE Select NP_444284.1:n.724-379C>A