Canonical Allele Identifier: CA381658061
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109191
MyVariant Identifiers: chr11:g.69462831T>A (hg19) chr11:g.69648063T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648063T>A , CM000673.2:g.69648063T>A GRCh38
NC_000011.9:g.69462831T>A , CM000673.1:g.69462831T>A GRCh37
NC_000011.8:g.69172012T>A NCBI36
NG_007375.1:g.11959T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.644T>A MANE Select ENSP00000227507.2:p.Leu215Gln
ENST00000227507.2:c.644T>A ENSP00000227507.2:p.Leu215Gln
ENST00000536559.1:c.*64T>A ENSP00000438482.1:n.*64T>A
ENST00000542367.1:n.107T>A
ENST00000545484.1:n.350T>A
NM_053056.2:c.644T>A NP_444284.1:p.Leu215Gln
XM_006718653.2:c.668T>A XP_006718716.1:p.Leu223Gln
NM_053056.3:c.644T>A MANE Select NP_444284.1:p.Leu215Gln
Search 100 bp 5'
Search 100 bp 3'