Canonical Allele Identifier: CA6156263
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs776600964
ExAC: 11:69462864 A / T
gnomAD v2: 11-69462864-A-T
gnomAD v4: 11-69648096-A-T
MyVariant Identifiers: chr11:g.69462864A>T (hg19) chr11:g.69648096A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648096A>T , CM000673.2:g.69648096A>T GRCh38
NC_000011.9:g.69462864A>T , CM000673.1:g.69462864A>T GRCh37
NC_000011.8:g.69172045A>T NCBI36
NG_007375.1:g.11992A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.677A>T MANE Select ENSP00000227507.2:p.Tyr226Phe
ENST00000227507.2:c.677A>T ENSP00000227507.2:p.Tyr226Phe
ENST00000536559.1:c.*97A>T ENSP00000438482.1:n.*97A>T
ENST00000542367.1:n.140A>T
ENST00000545484.1:n.383A>T
NM_053056.2:c.677A>T NP_444284.1:p.Tyr226Phe
XM_006718653.2:c.701A>T XP_006718716.1:p.Tyr234Phe
NM_053056.3:c.677A>T MANE Select NP_444284.1:p.Tyr226Phe
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