Canonical Allele Identifier: CA2574937219
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120108323
gnomAD v4: 11-69647958-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647958G>A , CM000673.2:g.69647958G>A GRCh38
NC_000011.9:g.69462726G>A , CM000673.1:g.69462726G>A GRCh37
NC_000011.8:g.69171907G>A NCBI36
NG_007375.1:g.11854G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-36G>A MANE Select ENSP00000227507.2:n.575-36G>A
ENST00000227507.2:c.575-36G>A ENSP00000227507.2:n.575-36G>A
ENST00000536559.1:c.199-36G>A ENSP00000438482.1:n.199-36G>A
ENST00000542367.1:n.2G>A
ENST00000545484.1:n.281-36G>A
NM_053056.2:c.575-36G>A NP_444284.1:n.575-36G>A
XM_006718653.2:c.599-36G>A XP_006718716.1:n.599-36G>A
NM_053056.3:c.575-36G>A MANE Select NP_444284.1:n.575-36G>A
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