Canonical Allele Identifier: CA381658145
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1222446202

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648101C>G , CM000673.2:g.69648101C>G GRCh38
NC_000011.9:g.69462869C>G , CM000673.1:g.69462869C>G GRCh37
NC_000011.8:g.69172050C>G NCBI36
NG_007375.1:g.11997C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.682C>G MANE Select ENSP00000227507.2:p.Arg228Gly
ENST00000227507.2:c.682C>G ENSP00000227507.2:p.Arg228Gly
ENST00000536559.1:c.*102C>G ENSP00000438482.1:n.*102C>G
ENST00000542367.1:n.145C>G
ENST00000545484.1:n.388C>G
NM_053056.2:c.682C>G NP_444284.1:p.Arg228Gly
XM_006718653.2:c.706C>G XP_006718716.1:p.Arg236Gly
NM_053056.3:c.682C>G MANE Select NP_444284.1:p.Arg228Gly