Canonical Allele Identifier: CA6156265
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs200179137
ExAC: 11:69462870 G / A
gnomAD v2: 11-69462870-G-A
gnomAD v3: 11-69648102-G-A
gnomAD v4: 11-69648102-G-A
MyVariant Identifiers: chr11:g.69462870G>A (hg19) chr11:g.69648102G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648102G>A , CM000673.2:g.69648102G>A GRCh38
NC_000011.9:g.69462870G>A , CM000673.1:g.69462870G>A GRCh37
NC_000011.8:g.69172051G>A NCBI36
NG_007375.1:g.11998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.683G>A MANE Select ENSP00000227507.2:p.Arg228His
ENST00000227507.2:c.683G>A ENSP00000227507.2:p.Arg228His
ENST00000536559.1:c.*103G>A ENSP00000438482.1:n.*103G>A
ENST00000542367.1:n.146G>A
ENST00000545484.1:n.389G>A
NM_053056.2:c.683G>A NP_444284.1:p.Arg228His
XM_006718653.2:c.707G>A XP_006718716.1:p.Arg236His
NM_053056.3:c.683G>A MANE Select NP_444284.1:p.Arg228His
Search 100 bp 5'
Search 100 bp 3'