Canonical Allele Identifier: CA381658142
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109693
MyVariant Identifiers: chr11:g.69462868C>A (hg19) chr11:g.69648100C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648100C>A , CM000673.2:g.69648100C>A GRCh38
NC_000011.9:g.69462868C>A , CM000673.1:g.69462868C>A GRCh37
NC_000011.8:g.69172049C>A NCBI36
NG_007375.1:g.11996C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.681C>A MANE Select ENSP00000227507.2:p.Tyr227Ter
ENST00000227507.2:c.681C>A ENSP00000227507.2:p.Tyr227Ter
ENST00000536559.1:c.*101C>A ENSP00000438482.1:n.*101C>A
ENST00000542367.1:n.144C>A
ENST00000545484.1:n.387C>A
NM_053056.2:c.681C>A NP_444284.1:p.Tyr227Ter
XM_006718653.2:c.705C>A XP_006718716.1:p.Tyr235Ter
NM_053056.3:c.681C>A MANE Select NP_444284.1:p.Tyr227Ter
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