Canonical Allele Identifier: CA2724204341
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs868741666
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69650051C>G , CM000673.2:g.69650051C>G GRCh38
NC_000011.9:g.69464819C>G , CM000673.1:g.69464819C>G GRCh37
NC_000011.8:g.69174000C>G NCBI36
NG_007375.1:g.13947C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-1067C>G MANE Select ENSP00000227507.2:n.724-1067C>G
ENST00000227507.2:c.724-1067C>G ENSP00000227507.2:n.724-1067C>G
ENST00000542367.1:n.187-1067C>G
NM_053056.2:c.724-1067C>G NP_444284.1:n.724-1067C>G
XM_006718653.2:c.748-1067C>G XP_006718716.1:n.748-1067C>G
NM_053056.3:c.724-1067C>G MANE Select NP_444284.1:n.724-1067C>G
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