Canonical Allele Identifier: CA381658194
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120110064
MyVariant Identifiers: chr11:g.69462893G>A (hg19) chr11:g.69648125G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648125G>A , CM000673.2:g.69648125G>A GRCh38
NC_000011.9:g.69462893G>A , CM000673.1:g.69462893G>A GRCh37
NC_000011.8:g.69172074G>A NCBI36
NG_007375.1:g.12021G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.706G>A MANE Select ENSP00000227507.2:p.Val236Met
ENST00000227507.2:c.706G>A ENSP00000227507.2:p.Val236Met
ENST00000536559.1:c.*126G>A ENSP00000438482.1:n.*126G>A
ENST00000542367.1:n.169G>A
ENST00000545484.1:n.412G>A
NM_053056.2:c.706G>A NP_444284.1:p.Val236Met
XM_006718653.2:c.730G>A XP_006718716.1:p.Val244Met
NM_053056.3:c.706G>A MANE Select NP_444284.1:p.Val236Met
Search 100 bp 5'
Search 100 bp 3'