Canonical Allele Identifier: CA475219581
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120110099
MyVariant Identifiers: chr11:g.69462895G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648127G>A , CM000673.2:g.69648127G>A GRCh38
NC_000011.9:g.69462895G>A , CM000673.1:g.69462895G>A GRCh37
NC_000011.8:g.69172076G>A NCBI36
NG_007375.1:g.12023G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.708G>A MANE Select ENSP00000227507.2:p.Val236=
ENST00000227507.2:c.708G>A ENSP00000227507.2:p.Val236=
ENST00000536559.1:c.*128G>A ENSP00000438482.1:n.*128G>A
ENST00000542367.1:n.171G>A
ENST00000545484.1:n.414G>A
NM_053056.2:c.708G>A NP_444284.1:p.Val236=
XM_006718653.2:c.732G>A XP_006718716.1:p.Val244=
NM_053056.3:c.708G>A MANE Select NP_444284.1:p.Val236=
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