Canonical Allele Identifier: CA475219584
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs773470948
MyVariant Identifiers: chr11:g.69462898C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648130C>A , CM000673.2:g.69648130C>A GRCh38
NC_000011.9:g.69462898C>A , CM000673.1:g.69462898C>A GRCh37
NC_000011.8:g.69172079C>A NCBI36
NG_007375.1:g.12026C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.711C>A MANE Select ENSP00000227507.2:p.Ile237=
ENST00000227507.2:c.711C>A ENSP00000227507.2:p.Ile237=
ENST00000536559.1:c.*131C>A ENSP00000438482.1:n.*131C>A
ENST00000542367.1:n.174C>A
ENST00000545484.1:n.417C>A
NM_053056.2:c.711C>A NP_444284.1:p.Ile237=
XM_006718653.2:c.735C>A XP_006718716.1:p.Ile245=
NM_053056.3:c.711C>A MANE Select NP_444284.1:p.Ile237=
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