Canonical Allele Identifier: CA381658197
Gene: CCND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69462894T>G (hg19) chr11:g.69648126T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648126T>G , CM000673.2:g.69648126T>G GRCh38
NC_000011.9:g.69462894T>G , CM000673.1:g.69462894T>G GRCh37
NC_000011.8:g.69172075T>G NCBI36
NG_007375.1:g.12022T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.707T>G MANE Select ENSP00000227507.2:p.Val236Gly
ENST00000227507.2:c.707T>G ENSP00000227507.2:p.Val236Gly
ENST00000536559.1:c.*127T>G ENSP00000438482.1:n.*127T>G
ENST00000542367.1:n.170T>G
ENST00000545484.1:n.413T>G
NM_053056.2:c.707T>G NP_444284.1:p.Val236Gly
XM_006718653.2:c.731T>G XP_006718716.1:p.Val244Gly
NM_053056.3:c.707T>G MANE Select NP_444284.1:p.Val236Gly
Search 100 bp 5'
Search 100 bp 3'