Canonical Allele Identifier: CA381658046
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109091

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648056C>G , CM000673.2:g.69648056C>G GRCh38
NC_000011.9:g.69462824C>G , CM000673.1:g.69462824C>G GRCh37
NC_000011.8:g.69172005C>G NCBI36
NG_007375.1:g.11952C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.637C>G MANE Select ENSP00000227507.2:p.Gln213Glu
ENST00000227507.2:c.637C>G ENSP00000227507.2:p.Gln213Glu
ENST00000536559.1:c.*57C>G ENSP00000438482.1:n.*57C>G
ENST00000542367.1:n.100C>G
ENST00000545484.1:n.343C>G
NM_053056.2:c.637C>G NP_444284.1:p.Gln213Glu
XM_006718653.2:c.661C>G XP_006718716.1:p.Gln221Glu
NM_053056.3:c.637C>G MANE Select NP_444284.1:p.Gln213Glu