Canonical Allele Identifier: CA6156258
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs747703578
ExAC: 11:69462846 C / T
gnomAD v2: 11-69462846-C-T
gnomAD v3: 11-69648078-C-T
gnomAD v4: 11-69648078-C-T
MyVariant Identifiers: chr11:g.69462846C>T (hg19) chr11:g.69648078C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648078C>T , CM000673.2:g.69648078C>T GRCh38
NC_000011.9:g.69462846C>T , CM000673.1:g.69462846C>T GRCh37
NC_000011.8:g.69172027C>T NCBI36
NG_007375.1:g.11974C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.659C>T MANE Select ENSP00000227507.2:p.Pro220Leu
ENST00000227507.2:c.659C>T ENSP00000227507.2:p.Pro220Leu
ENST00000536559.1:c.*79C>T ENSP00000438482.1:n.*79C>T
ENST00000542367.1:n.122C>T
ENST00000545484.1:n.365C>T
NM_053056.2:c.659C>T NP_444284.1:p.Pro220Leu
XM_006718653.2:c.683C>T XP_006718716.1:p.Pro228Leu
NM_053056.3:c.659C>T MANE Select NP_444284.1:p.Pro220Leu
Search 100 bp 5'
Search 100 bp 3'