Canonical Allele Identifier: CA475219569
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120109831
MyVariant Identifiers: chr11:g.69462877A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648109A>G , CM000673.2:g.69648109A>G GRCh38
NC_000011.9:g.69462877A>G , CM000673.1:g.69462877A>G GRCh37
NC_000011.8:g.69172058A>G NCBI36
NG_007375.1:g.12005A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.690A>G MANE Select ENSP00000227507.2:p.Thr230=
ENST00000227507.2:c.690A>G ENSP00000227507.2:p.Thr230=
ENST00000536559.1:c.*110A>G ENSP00000438482.1:n.*110A>G
ENST00000542367.1:n.153A>G
ENST00000545484.1:n.396A>G
NM_053056.2:c.690A>G NP_444284.1:p.Thr230=
XM_006718653.2:c.714A>G XP_006718716.1:p.Thr238=
NM_053056.3:c.690A>G MANE Select NP_444284.1:p.Thr230=
Search 100 bp 5'
Search 100 bp 3'