Canonical Allele Identifier: CA6156264
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs745585622
ExAC: 11:69462865 C / T
gnomAD v2: 11-69462865-C-T
gnomAD v3: 11-69648097-C-T
gnomAD v4: 11-69648097-C-T
MyVariant Identifiers: chr11:g.69462865C>T (hg19) chr11:g.69648097C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648097C>T , CM000673.2:g.69648097C>T GRCh38
NC_000011.9:g.69462865C>T , CM000673.1:g.69462865C>T GRCh37
NC_000011.8:g.69172046C>T NCBI36
NG_007375.1:g.11993C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.678C>T MANE Select ENSP00000227507.2:p.Tyr226=
ENST00000227507.2:c.678C>T ENSP00000227507.2:p.Tyr226=
ENST00000536559.1:c.*98C>T ENSP00000438482.1:n.*98C>T
ENST00000542367.1:n.141C>T
ENST00000545484.1:n.384C>T
NM_053056.2:c.678C>T NP_444284.1:p.Tyr226=
XM_006718653.2:c.702C>T XP_006718716.1:p.Tyr234=
NM_053056.3:c.678C>T MANE Select NP_444284.1:p.Tyr226=
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