Canonical Allele Identifier: CA600001784
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1261039036
gnomAD v2: 11-69463027-G-A
gnomAD v3: 11-69648259-G-A
gnomAD v4: 11-69648259-G-A
MyVariant Identifiers: chr11:g.69463027G>A (hg19) chr11:g.69648259G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648259G>A , CM000673.2:g.69648259G>A GRCh38
NC_000011.9:g.69463027G>A , CM000673.1:g.69463027G>A GRCh37
NC_000011.8:g.69172208G>A NCBI36
NG_007375.1:g.12155G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+117G>A MANE Select ENSP00000227507.2:n.723+117G>A
ENST00000227507.2:c.723+117G>A ENSP00000227507.2:n.723+117G>A
ENST00000542367.1:n.186+117G>A
NM_053056.2:c.723+117G>A NP_444284.1:n.723+117G>A
XM_006718653.2:c.747+117G>A XP_006718716.1:n.747+117G>A
NM_053056.3:c.723+117G>A MANE Select NP_444284.1:n.723+117G>A
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