Canonical Allele Identifier: CA381658187
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120110023
MyVariant Identifiers: chr11:g.69462891G>A (hg19) chr11:g.69648123G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648123G>A , CM000673.2:g.69648123G>A GRCh38
NC_000011.9:g.69462891G>A , CM000673.1:g.69462891G>A GRCh37
NC_000011.8:g.69172072G>A NCBI36
NG_007375.1:g.12019G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.704G>A MANE Select ENSP00000227507.2:p.Arg235Lys
ENST00000227507.2:c.704G>A ENSP00000227507.2:p.Arg235Lys
ENST00000536559.1:c.*124G>A ENSP00000438482.1:n.*124G>A
ENST00000542367.1:n.167G>A
ENST00000545484.1:n.410G>A
NM_053056.2:c.704G>A NP_444284.1:p.Arg235Lys
XM_006718653.2:c.728G>A XP_006718716.1:p.Arg243Lys
NM_053056.3:c.704G>A MANE Select NP_444284.1:p.Arg235Lys
Search 100 bp 5'
Search 100 bp 3'