Canonical Allele Identifier: CA223476443
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1006925787
gnomAD v3: 11-69650089-T-C
gnomAD v4: 11-69650089-T-C
MyVariant Identifiers: chr11:g.69464857T>C (hg19) chr11:g.69650089T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69650089T>C , CM000673.2:g.69650089T>C GRCh38
NC_000011.9:g.69464857T>C , CM000673.1:g.69464857T>C GRCh37
NC_000011.8:g.69174038T>C NCBI36
NG_007375.1:g.13985T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-1029T>C MANE Select ENSP00000227507.2:n.724-1029T>C
ENST00000227507.2:c.724-1029T>C ENSP00000227507.2:n.724-1029T>C
ENST00000542367.1:n.187-1029T>C
NM_053056.2:c.724-1029T>C NP_444284.1:n.724-1029T>C
XM_006718653.2:c.748-1029T>C XP_006718716.1:n.748-1029T>C
NM_053056.3:c.724-1029T>C MANE Select NP_444284.1:n.724-1029T>C
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