Canonical Allele Identifier: CA679683736
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1346275356

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69649941C>T , CM000673.2:g.69649941C>T GRCh38
NC_000011.9:g.69464709C>T , CM000673.1:g.69464709C>T GRCh37
NC_000011.8:g.69173890C>T NCBI36
NG_007375.1:g.13837C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-1177C>T MANE Select ENSP00000227507.2:n.724-1177C>T
ENST00000227507.2:c.724-1177C>T ENSP00000227507.2:n.724-1177C>T
ENST00000542367.1:n.187-1177C>T
NM_053056.2:c.724-1177C>T NP_444284.1:n.724-1177C>T
XM_006718653.2:c.748-1177C>T XP_006718716.1:n.748-1177C>T
NM_053056.3:c.724-1177C>T MANE Select NP_444284.1:n.724-1177C>T