Canonical Allele Identifier: CA381658188
Gene: CCND1 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.704G>C MANE Select ENSP00000227507.2:p.Arg235Thr
ENST00000227507.2:c.704G>C ENSP00000227507.2:p.Arg235Thr
ENST00000536559.1:c.*124G>C ENSP00000438482.1:n.*124G>C
ENST00000542367.1:n.167G>C
ENST00000545484.1:n.410G>C
NM_053056.2:c.704G>C NP_444284.1:p.Arg235Thr
XM_006718653.2:c.728G>C XP_006718716.1:p.Arg243Thr
NM_053056.3:c.704G>C MANE Select NP_444284.1:p.Arg235Thr
Search 100 bp 5'
Search 100 bp 3'