Canonical Allele Identifier: CA2614780069
Gene: CCND1 HGNC NCBI

Linked Data

gnomAD v4: 11-69648256-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648256C>A , CM000673.2:g.69648256C>A GRCh38
NC_000011.9:g.69463024C>A , CM000673.1:g.69463024C>A GRCh37
NC_000011.8:g.69172205C>A NCBI36
NG_007375.1:g.12152C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+114C>A MANE Select ENSP00000227507.2:n.723+114C>A
ENST00000227507.2:c.723+114C>A ENSP00000227507.2:n.723+114C>A
ENST00000542367.1:n.186+114C>A
NM_053056.2:c.723+114C>A NP_444284.1:n.723+114C>A
XM_006718653.2:c.747+114C>A XP_006718716.1:n.747+114C>A
NM_053056.3:c.723+114C>A MANE Select NP_444284.1:n.723+114C>A
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