Canonical Allele Identifier: CA939230691
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1262617521
gnomAD v3: 11-69648185-A-C
gnomAD v4: 11-69648185-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648185A>C , CM000673.2:g.69648185A>C GRCh38
NC_000011.9:g.69462953A>C , CM000673.1:g.69462953A>C GRCh37
NC_000011.8:g.69172134A>C NCBI36
NG_007375.1:g.12081A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+43A>C MANE Select ENSP00000227507.2:n.723+43A>C
ENST00000227507.2:c.723+43A>C ENSP00000227507.2:n.723+43A>C
ENST00000536559.1:c.*186A>C ENSP00000438482.1:n.*186A>C
ENST00000542367.1:n.186+43A>C
NM_053056.2:c.723+43A>C NP_444284.1:n.723+43A>C
XM_006718653.2:c.747+43A>C XP_006718716.1:n.747+43A>C
NM_053056.3:c.723+43A>C MANE Select NP_444284.1:n.723+43A>C
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