Canonical Allele Identifier: CA223474404
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs146267501

Genomic Alleles

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

Transcript Alleles

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