Canonical Allele Identifier: CA381658178
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109953
MyVariant Identifiers: chr11:g.69462885T>C (hg19) chr11:g.69648117T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648117T>C , CM000673.2:g.69648117T>C GRCh38
NC_000011.9:g.69462885T>C , CM000673.1:g.69462885T>C GRCh37
NC_000011.8:g.69172066T>C NCBI36
NG_007375.1:g.12013T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.698T>C MANE Select ENSP00000227507.2:p.Leu233Pro
ENST00000227507.2:c.698T>C ENSP00000227507.2:p.Leu233Pro
ENST00000536559.1:c.*118T>C ENSP00000438482.1:n.*118T>C
ENST00000542367.1:n.161T>C
ENST00000545484.1:n.404T>C
NM_053056.2:c.698T>C NP_444284.1:p.Leu233Pro
XM_006718653.2:c.722T>C XP_006718716.1:p.Leu241Pro
NM_053056.3:c.698T>C MANE Select NP_444284.1:p.Leu233Pro
Search 100 bp 5'
Search 100 bp 3'