Canonical Allele Identifier: CA381658175
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1228811654
MyVariant Identifiers: chr11:g.69462884C>G (hg19) chr11:g.69648116C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648116C>G , CM000673.2:g.69648116C>G GRCh38
NC_000011.9:g.69462884C>G , CM000673.1:g.69462884C>G GRCh37
NC_000011.8:g.69172065C>G NCBI36
NG_007375.1:g.12012C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.697C>G MANE Select ENSP00000227507.2:p.Leu233Val
ENST00000227507.2:c.697C>G ENSP00000227507.2:p.Leu233Val
ENST00000536559.1:c.*117C>G ENSP00000438482.1:n.*117C>G
ENST00000542367.1:n.160C>G
ENST00000545484.1:n.403C>G
NM_053056.2:c.697C>G NP_444284.1:p.Leu233Val
XM_006718653.2:c.721C>G XP_006718716.1:p.Leu241Val
NM_053056.3:c.697C>G MANE Select NP_444284.1:p.Leu233Val
Search 100 bp 5'
Search 100 bp 3'