Canonical Allele Identifier: CA381658056
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109150
MyVariant Identifiers: chr11:g.69462828G>A (hg19) chr11:g.69648060G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648060G>A , CM000673.2:g.69648060G>A GRCh38
NC_000011.9:g.69462828G>A , CM000673.1:g.69462828G>A GRCh37
NC_000011.8:g.69172009G>A NCBI36
NG_007375.1:g.11956G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.641G>A MANE Select ENSP00000227507.2:p.Gly214Asp
ENST00000227507.2:c.641G>A ENSP00000227507.2:p.Gly214Asp
ENST00000536559.1:c.*61G>A ENSP00000438482.1:n.*61G>A
ENST00000542367.1:n.104G>A
ENST00000545484.1:n.347G>A
NM_053056.2:c.641G>A NP_444284.1:p.Gly214Asp
XM_006718653.2:c.665G>A XP_006718716.1:p.Gly222Asp
NM_053056.3:c.641G>A MANE Select NP_444284.1:p.Gly214Asp
Search 100 bp 5'
Search 100 bp 3'