Canonical Allele Identifier: CA381658137
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109660
gnomAD v4: 11-69648098-T-C
MyVariant Identifiers: chr11:g.69462866T>C (hg19) chr11:g.69648098T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648098T>C , CM000673.2:g.69648098T>C GRCh38
NC_000011.9:g.69462866T>C , CM000673.1:g.69462866T>C GRCh37
NC_000011.8:g.69172047T>C NCBI36
NG_007375.1:g.11994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.679T>C MANE Select ENSP00000227507.2:p.Tyr227His
ENST00000227507.2:c.679T>C ENSP00000227507.2:p.Tyr227His
ENST00000536559.1:c.*99T>C ENSP00000438482.1:n.*99T>C
ENST00000542367.1:n.142T>C
ENST00000545484.1:n.385T>C
NM_053056.2:c.679T>C NP_444284.1:p.Tyr227His
XM_006718653.2:c.703T>C XP_006718716.1:p.Tyr235His
NM_053056.3:c.679T>C MANE Select NP_444284.1:p.Tyr227His
Search 100 bp 5'
Search 100 bp 3'