Canonical Allele Identifier: CA381658116
Gene: CCND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69462855T>G (hg19) chr11:g.69648087T>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.668T>G MANE Select ENSP00000227507.2:p.Phe223Cys
ENST00000227507.2:c.668T>G ENSP00000227507.2:p.Phe223Cys
ENST00000536559.1:c.*88T>G ENSP00000438482.1:n.*88T>G
ENST00000542367.1:n.131T>G
ENST00000545484.1:n.374T>G
NM_053056.2:c.668T>G NP_444284.1:p.Phe223Cys
XM_006718653.2:c.692T>G XP_006718716.1:p.Phe231Cys
NM_053056.3:c.668T>G MANE Select NP_444284.1:p.Phe223Cys
Search 100 bp 5'
Search 100 bp 3'