Canonical Allele Identifier: CA475219509
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120108774
MyVariant Identifiers: chr11:g.69462790C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648022C>G , CM000673.2:g.69648022C>G GRCh38
NC_000011.9:g.69462790C>G , CM000673.1:g.69462790C>G GRCh37
NC_000011.8:g.69171971C>G NCBI36
NG_007375.1:g.11918C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.603C>G MANE Select ENSP00000227507.2:p.Ser201=
ENST00000227507.2:c.603C>G ENSP00000227507.2:p.Ser201=
ENST00000536559.1:c.*23C>G ENSP00000438482.1:n.*23C>G
ENST00000542367.1:n.66C>G
ENST00000545484.1:n.309C>G
NM_053056.2:c.603C>G NP_444284.1:p.Ser201=
XM_006718653.2:c.627C>G XP_006718716.1:p.Ser209=
NM_053056.3:c.603C>G MANE Select NP_444284.1:p.Ser201=
Search 100 bp 5'
Search 100 bp 3'