Canonical Allele Identifier: CA6156260
Gene: CCND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1250573
ClinVar RCV Id: RCV001652823 RCV003968426
dbSNP Id: rs3862792
ExAC: 11:69462856 C / T
gnomAD v2: 11-69462856-C-T
gnomAD v3: 11-69648088-C-T
gnomAD v4: 11-69648088-C-T
MyVariant Identifiers: chr11:g.69462856C>T (hg19) chr11:g.69648088C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648088C>T , CM000673.2:g.69648088C>T GRCh38
NC_000011.9:g.69462856C>T , CM000673.1:g.69462856C>T GRCh37
NC_000011.8:g.69172037C>T NCBI36
NG_007375.1:g.11984C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.669C>T MANE Select ENSP00000227507.2:p.Phe223=
ENST00000227507.2:c.669C>T ENSP00000227507.2:p.Phe223=
ENST00000536559.1:c.*89C>T ENSP00000438482.1:n.*89C>T
ENST00000542367.1:n.132C>T
ENST00000545484.1:n.375C>T
NM_053056.2:c.669C>T NP_444284.1:p.Phe223=
XM_006718653.2:c.693C>T XP_006718716.1:p.Phe231=
NM_053056.3:c.669C>T MANE Select NP_444284.1:p.Phe223=
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Search 100 bp 3'