Canonical Allele Identifier: CA381658115
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109511
MyVariant Identifiers: chr11:g.69462855T>C (hg19) chr11:g.69648087T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648087T>C , CM000673.2:g.69648087T>C GRCh38
NC_000011.9:g.69462855T>C , CM000673.1:g.69462855T>C GRCh37
NC_000011.8:g.69172036T>C NCBI36
NG_007375.1:g.11983T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.668T>C MANE Select ENSP00000227507.2:p.Phe223Ser
ENST00000227507.2:c.668T>C ENSP00000227507.2:p.Phe223Ser
ENST00000536559.1:c.*88T>C ENSP00000438482.1:n.*88T>C
ENST00000542367.1:n.131T>C
ENST00000545484.1:n.374T>C
NM_053056.2:c.668T>C NP_444284.1:p.Phe223Ser
XM_006718653.2:c.692T>C XP_006718716.1:p.Phe231Ser
NM_053056.3:c.668T>C MANE Select NP_444284.1:p.Phe223Ser
Search 100 bp 5'
Search 100 bp 3'