Canonical Allele Identifier: CA475219559
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109589
MyVariant Identifiers: chr11:g.69462862C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648094C>G , CM000673.2:g.69648094C>G GRCh38
NC_000011.9:g.69462862C>G , CM000673.1:g.69462862C>G GRCh37
NC_000011.8:g.69172043C>G NCBI36
NG_007375.1:g.11990C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.675C>G MANE Select ENSP00000227507.2:p.Ser225=
ENST00000227507.2:c.675C>G ENSP00000227507.2:p.Ser225=
ENST00000536559.1:c.*95C>G ENSP00000438482.1:n.*95C>G
ENST00000542367.1:n.138C>G
ENST00000545484.1:n.381C>G
NM_053056.2:c.675C>G NP_444284.1:p.Ser225=
XM_006718653.2:c.699C>G XP_006718716.1:p.Ser233=
NM_053056.3:c.675C>G MANE Select NP_444284.1:p.Ser225=
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