Canonical Allele Identifier: CA475219528
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs146267501
MyVariant Identifiers: chr11:g.69462817C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648049C>A , CM000673.2:g.69648049C>A GRCh38
NC_000011.9:g.69462817C>A , CM000673.1:g.69462817C>A GRCh37
NC_000011.8:g.69171998C>A NCBI36
NG_007375.1:g.11945C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.630C>A MANE Select ENSP00000227507.2:p.Ala210=
ENST00000227507.2:c.630C>A ENSP00000227507.2:p.Ala210=
ENST00000536559.1:c.*50C>A ENSP00000438482.1:n.*50C>A
ENST00000542367.1:n.93C>A
ENST00000545484.1:n.336C>A
NM_053056.2:c.630C>A NP_444284.1:p.Ala210=
XM_006718653.2:c.654C>A XP_006718716.1:p.Ala218=
NM_053056.3:c.630C>A MANE Select NP_444284.1:p.Ala210=