Canonical Allele Identifier: CA223474510
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs773470948

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648130C>G , CM000673.2:g.69648130C>G GRCh38
NC_000011.9:g.69462898C>G , CM000673.1:g.69462898C>G GRCh37
NC_000011.8:g.69172079C>G NCBI36
NG_007375.1:g.12026C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.711C>G MANE Select ENSP00000227507.2:p.Ile237Met
ENST00000227507.2:c.711C>G ENSP00000227507.2:p.Ile237Met
ENST00000536559.1:c.*131C>G ENSP00000438482.1:n.*131C>G
ENST00000542367.1:n.174C>G
ENST00000545484.1:n.417C>G
NM_053056.2:c.711C>G NP_444284.1:p.Ile237Met
XM_006718653.2:c.735C>G XP_006718716.1:p.Ile245Met
NM_053056.3:c.711C>G MANE Select NP_444284.1:p.Ile237Met