Canonical Allele Identifier: CA475219555
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs770661706
MyVariant Identifiers: chr11:g.69462859G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648091G>A , CM000673.2:g.69648091G>A GRCh38
NC_000011.9:g.69462859G>A , CM000673.1:g.69462859G>A GRCh37
NC_000011.8:g.69172040G>A NCBI36
NG_007375.1:g.11987G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.672G>A MANE Select ENSP00000227507.2:p.Leu224=
ENST00000227507.2:c.672G>A ENSP00000227507.2:p.Leu224=
ENST00000536559.1:c.*92G>A ENSP00000438482.1:n.*92G>A
ENST00000542367.1:n.135G>A
ENST00000545484.1:n.378G>A
NM_053056.2:c.672G>A NP_444284.1:p.Leu224=
XM_006718653.2:c.696G>A XP_006718716.1:p.Leu232=
NM_053056.3:c.672G>A MANE Select NP_444284.1:p.Leu224=
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Search 100 bp 3'