Canonical Allele Identifier: CA2598689051
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120115842
gnomAD v3: 11-69650005-G-A
gnomAD v4: 11-69650005-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69650005G>A , CM000673.2:g.69650005G>A GRCh38
NC_000011.9:g.69464773G>A , CM000673.1:g.69464773G>A GRCh37
NC_000011.8:g.69173954G>A NCBI36
NG_007375.1:g.13901G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.724-1113G>A MANE Select ENSP00000227507.2:n.724-1113G>A
ENST00000227507.2:c.724-1113G>A ENSP00000227507.2:n.724-1113G>A
ENST00000542367.1:n.187-1113G>A
NM_053056.2:c.724-1113G>A NP_444284.1:n.724-1113G>A
XM_006718653.2:c.748-1113G>A XP_006718716.1:n.748-1113G>A
NM_053056.3:c.724-1113G>A MANE Select NP_444284.1:n.724-1113G>A
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